AiPD: Autoinhibited Protein Database

P82912

Gene name	MRPS11
Protein name	28S ribosomal protein S11, mitochondrial
Names	MRP-S11, S11mt, Cervical cancer proto-oncogene 2 protein, HCC-2, Mitochondrial small ribosomal subunit protein uS11m
Species	Homo sapiens (Human)
KEGG Pathway	hsa:64963
EC number
Protein Class

Descriptions

The autoinhibited protein was predicted that may have potential autoinhibitory elements via cis-regPred.

Autoinhibitory domains (AIDs)

88-157 (Predicted disordered autoinhibitory region) PR

Target domain
Relief mechanism
Assay	cis-regPred

AID

88-157 (Predicted disordered autoinhibitory region)

Target domain

Relief mechanism

Assay

cis-regPred

Accessory elements

No accessory elements

References

Yeon JH et al. (2016) "Systems-wide Identification of cis-Regulatory Elements in Proteins", Cell Systems, 2, 89-100

Autoinhibited structure

Activated structure

41 structures for P82912

Entry ID	Method	Resolution	Chain	Position	Source
3J9M	EM	350 A	AI	1-194	PDB
6NU2	EM	390 A	AI	59-194	PDB
6NU3	EM	440 A	AI	1-194	PDB
6RW4	EM	297 A	I	1-194	PDB
6RW5	EM	314 A	I	1-194	PDB
6VLZ	EM	297 A	AI	1-194	PDB
6VMI	EM	296 A	AI	1-194	PDB
6ZM5	EM	289 A	AI	1-194	PDB
6ZM6	EM	259 A	AI	1-194	PDB
6ZS9	EM	400 A	AI	1-194	PDB
6ZSA	EM	400 A	AI	1-194	PDB
6ZSB	EM	450 A	AI	1-194	PDB
6ZSC	EM	350 A	AI	1-194	PDB
6ZSD	EM	370 A	AI	1-194	PDB
6ZSE	EM	500 A	AI	1-194	PDB
6ZSG	EM	400 A	AI	1-194	PDB
7A5F	EM	440 A	I6	1-194	PDB
7A5G	EM	433 A	I6	1-194	PDB
7A5I	EM	370 A	I6	1-194	PDB
7A5K	EM	370 A	I6	1-194	PDB
7L08	EM	349 A	AI	1-194	PDB
7OG4	EM	380 A	AI	1-194	PDB
7P2E	EM	240 A	I	1-194	PDB
7PNX	EM	276 A	I	1-194	PDB
7PNY	EM	306 A	I	1-194	PDB
7PNZ	EM	309 A	I	1-194	PDB
7PO0	EM	290 A	I	1-194	PDB
7PO1	EM	292 A	I	1-194	PDB
7PO2	EM	309 A	I	1-194	PDB
7PO3	EM	292 A	I	1-194	PDB
7QI4	EM	221 A	AI	1-194	PDB
7QI5	EM	263 A	AI	1-194	PDB
7QI6	EM	298 A	AI	1-194	PDB
8ANY	EM	285 A	AI	1-194	PDB
8CSR	EM	254 A	I	1-194	PDB
8CSS	EM	236 A	I	1-194	PDB
8CST	EM	285 A	I	1-194	PDB
8CSU	EM	303 A	I	1-194	PDB
8OIR	EM	310 A	Ai	1-194	PDB
8OIS	EM	300 A	Ai	1-194	PDB
AF-P82912-F1	Predicted				AlphaFoldDB

179 variants for P82912

Variant ID(s)	Position	Change	Description	Diseaes Association	Provenance
CA393704977 rs1382971423	2	Q>E		No	ClinGen gnomAD
CA7717746 rs199864572	3	A>T		No	ClinGen 1000Genomes ExAC TOPMed gnomAD
CA393705005 rs1363073925	4	V>A		No	ClinGen gnomAD
CA7717747 rs371970512	6	N>I		No	ClinGen ESP ExAC gnomAD
CA7717748 rs763313554	7	A>P		No	ClinGen ExAC gnomAD
rs144247178 CA7717749	7	A>V		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
rs185895652 CA7717752	8	G>E		No	ClinGen 1000Genomes ExAC TOPMed gnomAD
rs148734646 CA7717750	8	G>R		No	ClinGen ESP ExAC TOPMed gnomAD
rs185895652 CA7717751	8	G>V		No	ClinGen 1000Genomes ExAC TOPMed gnomAD
CA274454458 rs201980995	9	S>*		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
CA7717753 rs201980995	9	S>L		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
CA274454454 rs201980995	9	S>W		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
rs905375225 CA274454472	10	R>L		No	ClinGen TOPMed gnomAD
rs905375225 CA274454471	10	R>Q		No	ClinGen TOPMed gnomAD
rs16941904 VAR_052054 CA7717755	10	R>W		No	ClinGen UniProt 1000Genomes ESP ExAC TOPMed dbSNP gnomAD
CA393705078 rs1236009202	11	F>C		No	ClinGen TOPMed
CA7717757 rs758094710	11	F>L		No	ClinGen ExAC TOPMed gnomAD
rs1598286787 CA393705075	11	F>V		No	ClinGen Ensembl
CA7717758 rs777109331	12	L>R		No	ClinGen ExAC gnomAD
CA393705100 rs1160450951	13	R>Q		No	ClinGen TOPMed gnomAD
rs1454535143 CA393705098	13	R>W		No	ClinGen gnomAD
rs781761457 CA7717761	15	W>R		No	ClinGen ExAC gnomAD
CA393705133 rs1370801929	16	T>A		No	ClinGen gnomAD
rs867329734 CA274454520	17	W>*		No	ClinGen Ensembl
CA7717762 rs746417496	17	W>R		No	ClinGen ExAC
rs1567041956 CA393705168	18	P>L		No	ClinGen Ensembl
CA393705160 rs1320646142	18	P>T		No	ClinGen TOPMed
rs1326622020 CA393705174	19	Q>*		No	ClinGen TOPMed gnomAD
rs770260993 CA7717763	20	T>A		No	ClinGen ExAC TOPMed gnomAD
CA393705190 rs1384955838	20	T>I		No	ClinGen TOPMed gnomAD
CA393705191 rs1285644706	21	A>T		No	ClinGen TOPMed
rs201087926 CA7717764	22	G>R		No	ClinGen ESP ExAC TOPMed gnomAD
CA393705197 rs201087926	22	G>S		No	ClinGen ESP ExAC TOPMed gnomAD
CA393705266 rs748362898	23	R>S		No	ClinGen ExAC TOPMed gnomAD
rs772119585 CA7717788	24	V>F		No	ClinGen ExAC gnomAD
rs772119585 CA393705277	24	V>I		No	ClinGen ExAC gnomAD
CA274454680 rs892806502	26	A>D		No	ClinGen gnomAD
CA393705317 rs892806502	26	A>V		No	ClinGen gnomAD
rs199770606 CA274454694	27	R>G		No	ClinGen ExAC TOPMed gnomAD
CA7717791 rs769728154	29	P>S		No	ClinGen ExAC gnomAD
rs775090003 CA7717792	30	A>T		No	ClinGen ExAC gnomAD
rs762797699 CA7717793	30	A>V	Variant assessed as Somatic; 0.0 impact. [NCI-TCGA]	No	ClinGen ExAC NCI-TCGA gnomAD
rs763862491 CA7717794	31	G>R		No	ClinGen ExAC TOPMed gnomAD
rs763862491 CA393705399	31	G>W		No	ClinGen ExAC TOPMed gnomAD
rs1341825392 CA393705411	32	T>A		No	ClinGen gnomAD
rs774031538 CA7717797	35	T>R		No	ClinGen ExAC TOPMed gnomAD
CA393705490 rs1262461691	36	G>D		No	ClinGen gnomAD
rs756628463 CA7717801	37	A>G		No	ClinGen ExAC gnomAD
CA7717800 rs749957719	37	A>S		No	ClinGen ExAC gnomAD
rs754366970 COSM1740192 CA7717803	38	R>*	haematopoietic_and_lymphoid_tissue [Cosmic]	No	ClinGen cosmic curated ExAC TOPMed gnomAD
CA393705528 rs1357114480	38	R>Q		No	ClinGen gnomAD
rs1409200709 CA393705538	39	Q>E		No	ClinGen TOPMed
CA7717805 rs779197417	39	Q>R		No	ClinGen ExAC TOPMed gnomAD
CA274454730 rs576217619	40	L>P		No	ClinGen 1000Genomes
CA7717806 rs748355847	41	Q>R		No	ClinGen ExAC gnomAD
CA393705585 rs1296107575	42	D>N		No	ClinGen gnomAD
rs777764544 CA393705612	43	A>G		No	ClinGen ExAC gnomAD
rs777764544 CA7717808	43	A>V		No	ClinGen ExAC gnomAD
CA393705647 rs1281151821	45	A>G		No	ClinGen gnomAD
rs372077725 CA7717809	45	A>T		No	ClinGen ExAC TOPMed gnomAD
rs1222656354 CA393705723	50	E>Q		No	ClinGen TOPMed
CA393705734 rs147602817	51	Q>*		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
VAR_052055 rs16941907 CA7717813	51	Q>H		No	ClinGen UniProt 1000Genomes ESP ExAC TOPMed dbSNP gnomAD
CA7717811 rs147602817	51	Q>K		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
CA7717812 rs749231754	51	Q>L		No	ClinGen ExAC TOPMed gnomAD
TCGA novel	51	Q>R	Variant assessed as Somatic; impact. [NCI-TCGA]	No	NCI-TCGA
rs1035236987 CA274454753	52	N>I		No	ClinGen Ensembl
CA393705750 rs1035236987	52	N>T		No	ClinGen Ensembl
rs761489372 CA7717815	54	A>D		No	ClinGen ExAC TOPMed gnomAD
rs761489372 CA7717816	54	A>V		No	ClinGen ExAC TOPMed gnomAD
rs1422718585 CA393705820	56	S>N		No	ClinGen gnomAD
CA7717818 rs760254324	57	H>P		No	ClinGen ExAC gnomAD
CA393705868 rs1455225205	58	T>I		No	ClinGen gnomAD
TCGA novel	59	K>E	Variant assessed as Somatic; impact. [NCI-TCGA]	No	NCI-TCGA
CA393705896 rs1365178211	60	F>S		No	ClinGen gnomAD
rs1405671286 CA393705891	60	F>V		No	ClinGen TOPMed
CA393706977 rs1337858563	61	S>R		No	ClinGen TOPMed
CA393706991 rs1473519704	63	Y>C		No	ClinGen gnomAD
rs765677167 CA7717842	64	P>L		No	ClinGen ExAC TOPMed gnomAD
CA393707009 rs1412345112	66	I>T		No	ClinGen gnomAD
rs753261109 CA7717843	67	P>S	Variant assessed as Somatic; 0.0 impact. [NCI-TCGA]	No	ClinGen ExAC NCI-TCGA gnomAD
rs1166452551 CA393707036	70	E>G		No	ClinGen TOPMed
CA393707040 rs1567044855	71	S>G		No	ClinGen Ensembl
rs1372759858 CA393707042	71	S>N		No	ClinGen gnomAD
rs995631744 CA274457353	74	R>K		No	ClinGen TOPMed
rs763305607 CA7717845	75	W>*		No	ClinGen ExAC gnomAD
rs1307714838 CA393707076	76	A>G		No	ClinGen TOPMed gnomAD
rs1307714838 CA393707077	76	A>V		No	ClinGen TOPMed gnomAD
COSM3741717 CA274457364 rs951473750	77	G>E	liver [Cosmic]	No	ClinGen cosmic curated TOPMed gnomAD
CA393707091 rs1282487287	79	K>*		No	ClinGen gnomAD
rs751729742 CA7717848	84	P>L		No	ClinGen ExAC gnomAD
CA7717847 rs751729742	84	P>R		No	ClinGen ExAC gnomAD
CA393707137 rs1215019531	85	I>F		No	ClinGen TOPMed gnomAD
CA393707136 rs1215019531	85	I>V		No	ClinGen TOPMed gnomAD
CA393707158 rs1466664043	88	I>V		No	ClinGen gnomAD
CA274457379 rs200489584	89	K>R		No	ClinGen 1000Genomes
CA393707184 rs1204145967	92	H>Y		No	ClinGen TOPMed gnomAD
CA7717851 rs756271529	93	N>D		No	ClinGen ExAC gnomAD
rs778708096 CA7717852	93	N>S		No	ClinGen ExAC gnomAD
rs766611176 CA7717870	97	I>T		No	ClinGen ExAC gnomAD
rs372888234 CA393707320	99	V>I		No	ClinGen ESP ExAC TOPMed gnomAD
CA7717872 rs372888234	99	V>L		No	ClinGen ESP ExAC TOPMed gnomAD
rs774759448 CA274458625	100	V>I		No	ClinGen Ensembl
rs1434198643 CA393707338	101	S>P		No	ClinGen gnomAD
rs1030402614 CA274458632	102	A>P		No	ClinGen TOPMed gnomAD
CA274458640 rs150288962	103	S>G		No	ClinGen ESP TOPMed gnomAD
CA393707382 rs1230767838	105	E>K		No	ClinGen gnomAD
CA7717876 rs144899922	106	P>S		No	ClinGen ESP ExAC TOPMed gnomAD
rs769166605 CA7717878	108	A>T		No	ClinGen ExAC gnomAD
rs988867505 CA274458674	108	A>V	Variant assessed as Somatic; 0.0 impact. [NCI-TCGA]	No	ClinGen NCI-TCGA TOPMed gnomAD
CA274458678 rs913217976	111	S>F		No	ClinGen TOPMed gnomAD
CA393707449 rs1268519798	112	C>Y		No	ClinGen TOPMed gnomAD
rs1293117716 CA393707460	113	G>C		No	ClinGen TOPMed
rs577243785 CA7717881	114	T>I		No	ClinGen 1000Genomes ExAC gnomAD
rs1377348091 CA393707479	115	E>*		No	ClinGen gnomAD
rs748353445 CA393707486	115	E>D		No	ClinGen gnomAD
CA7717883 COSM197647 rs774896757	118	R>Q	Variant assessed as Somatic; 0.0 impact. large_intestine [NCI-TCGA, Cosmic]	No	ClinGen cosmic curated ExAC NCI-TCGA TOPMed gnomAD
CA7717882 COSM197646 rs149047976	118	R>W	Variant assessed as Somatic; 0.0 impact. large_intestine [NCI-TCGA, Cosmic]	No	ClinGen cosmic curated ESP ExAC NCI-TCGA TOPMed gnomAD
rs544573681 CA7717884	119	N>S		No	ClinGen 1000Genomes ExAC gnomAD
CA393707566 rs1384932069	123	G>D		No	ClinGen gnomAD
COSM300090 CA7717889 rs753974502	127	A>T	large_intestine [Cosmic]	No	ClinGen cosmic curated ExAC TOPMed gnomAD
CA7717890 rs758357205	127	A>V		No	ClinGen ExAC gnomAD
rs764119093 CA7717891	128	A>T		No	ClinGen ExAC gnomAD
TCGA novel	131	A>G	Variant assessed as Somatic; impact. [NCI-TCGA]	No	NCI-TCGA
CA7717892 rs376856888	133	I>L		No	ClinGen ESP ExAC TOPMed gnomAD
CA7717893 rs376856888	133	I>V		No	ClinGen ESP ExAC TOPMed gnomAD
rs138959508 CA393707681	135	A>S		No	ClinGen ESP ExAC TOPMed gnomAD
rs138959508 CA7717895	135	A>T		No	ClinGen ESP ExAC TOPMed gnomAD
rs142183271 CA7717896	135	A>V		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
CA7717897 rs779480334	136	A>V		No	ClinGen ExAC TOPMed gnomAD
rs779356539 CA7717900	137	A>=	Variant assessed as Somatic; 0.0 impact. [NCI-TCGA]	No	ClinGen ExAC NCI-TCGA TOPMed gnomAD
rs561515348 CA7717899	137	A>V		No	ClinGen 1000Genomes ExAC TOPMed gnomAD
rs748561221 CA7717923	139	A>T		No	ClinGen ExAC TOPMed gnomAD
rs1366556636 CA393708187	141	Q>*		No	ClinGen TOPMed gnomAD
rs1366556636 CA393708186	141	Q>E		No	ClinGen TOPMed gnomAD
rs772639439 CA7717924	141	Q>L		No	ClinGen ExAC gnomAD
CA7717925 rs777945324	143	G>S		No	ClinGen ExAC TOPMed gnomAD
rs753118687 CA7717928	144	V>M		No	ClinGen ExAC TOPMed gnomAD
rs1357311338 CA393708210	145	I>L		No	ClinGen TOPMed
rs759886427 COSM966185 CA7717930	148	R>*	Variant assessed as Somatic; 0.0 impact. endometrium [NCI-TCGA, Cosmic]	No	ClinGen cosmic curated ExAC NCI-TCGA TOPMed gnomAD
rs759886427 CA7717929	148	R>G		No	ClinGen ExAC TOPMed gnomAD
CA274459762 rs868558983	148	R>Q		No	ClinGen TOPMed gnomAD
rs775672598 CA7717931	149	V>L		No	ClinGen ExAC gnomAD
rs138464643 CA7717933	151	V>M		No	ClinGen ESP ExAC gnomAD
CA7717934 rs142017223	158	R>C		No	ClinGen ESP ExAC TOPMed gnomAD
CA7717935 rs750394239	158	R>H		No	ClinGen ExAC gnomAD
CA274460122 rs954122257	161	A>V		No	ClinGen TOPMed
rs1459306984 CA393708322	162	M>V		No	ClinGen gnomAD
CA393708355 rs115165544	163	H>Q		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
CA7717954 COSM1375245 rs372417211	164	G>R	large_intestine [Cosmic]	No	ClinGen cosmic curated ESP ExAC TOPMed gnomAD
CA7717955 rs766119679	165	L>P		No	ClinGen ExAC gnomAD
CA393708387 rs1415529603	166	I>N		No	ClinGen TOPMed
CA7717956 rs776412088	166	I>V		No	ClinGen ExAC TOPMed gnomAD
rs1223060248 CA393708415	168	G>D		No	ClinGen gnomAD
rs201886790 CA7717958	169	G>S		No	ClinGen ESP ExAC TOPMed gnomAD
CA393708432 rs1390427136	170	L>M		No	ClinGen TOPMed
CA7717960 rs757898412	171	E>*		No	ClinGen ExAC TOPMed gnomAD
rs139694172 CA7717961 CA7717962	171	E>D		No	ClinGen ESP ExAC TOPMed gnomAD
CA393708464 rs1223517257	173	I>L		No	ClinGen gnomAD
rs1490093599 CA393708475	173	I>M		No	ClinGen gnomAD
CA393708473 rs1244699342	173	I>S		No	ClinGen gnomAD
rs149376629 CA7717963	175	I>V		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
CA393708537 rs1437169391	179	T>A		No	ClinGen TOPMed
CA393708540 rs1437169391	179	T>P		No	ClinGen TOPMed
CA274460186 rs916367056	180	P>A		No	ClinGen gnomAD
CA393708551 rs916367056	180	P>S		No	ClinGen gnomAD
rs746219535 CA7717965	181	I>V		No	ClinGen ExAC gnomAD
CA393708597 rs1167352801	184	N>D		No	ClinGen gnomAD
rs147493631 CA274460192	184	N>S		No	ClinGen ESP TOPMed
CA7717967 rs369601980	185	G>S		No	ClinGen ESP ExAC TOPMed gnomAD
rs1598297488 CA393708630	186	C>W		No	ClinGen Ensembl
rs749517118 CA7717968	187	R>C		No	ClinGen ExAC TOPMed gnomAD
CA7717969 rs144441447	187	R>H		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
rs147829843 CA393708693	192	R>G		No	ClinGen ESP ExAC TOPMed gnomAD
CA274460208 rs139450964	192	R>P		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
CA7717971 rs139450964	192	R>Q		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
CA7717970 rs147829843	192	R>W		No	ClinGen ESP ExAC TOPMed gnomAD
rs754176735 CA7717972	193	K>R		No	ClinGen ExAC gnomAD
CA393708725 rs1358528668	195	L>R		No	ClinGen gnomAD

No associated diseases with P82912

1 regional properties for P82912

Type	Name	Position	InterPro Accession
conserved_site	Ribosomal S11, conserved site	162 - 184	IPR018102

Functions

		Description
EC Number
Subcellular Localization	Mitochondrion
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category	No pathway information available

4 GO annotations of cellular component

Name	Definition
cytosolic small ribosomal subunit	The small subunit of a ribosome located in the cytosol.
mitochondrial inner membrane	The inner, i.e. lumen-facing, lipid bilayer of the mitochondrial envelope. It is highly folded to form cristae.
mitochondrial small ribosomal subunit	The smaller of the two subunits of a mitochondrial ribosome.
mitochondrion	A semiautonomous, self replicating organelle that occurs in varying numbers, shapes, and sizes in the cytoplasm of virtually all eukaryotic cells. It is notably the site of tissue respiration.

4 GO annotations of molecular function

Name	Definition
mRNA 5'-UTR binding	Binding to an mRNA molecule at its 5' untranslated region.
RNA binding	Binding to an RNA molecule or a portion thereof.
small ribosomal subunit rRNA binding	Binding to small ribosomal subunit RNA (SSU rRNA), a constituent of the small ribosomal subunit. In S. cerevisiae, this is the 18S rRNA.
structural constituent of ribosome	The action of a molecule that contributes to the structural integrity of the ribosome.

4 GO annotations of biological process

Name	Definition
maturation of SSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA)	Any process involved in the maturation of a precursor Small SubUnit (SSU) ribosomal RNA (rRNA) molecule into a mature SSU-rRNA molecule from the pre-rRNA molecule originally produced as a tricistronic rRNA transcript that contains the Small Subunit (SSU) rRNA, 5.8S rRNA, and the Large Subunit (LSU) in that order from 5' to 3' along the primary transcript.
mitochondrial translation	The chemical reactions and pathways resulting in the formation of a protein in a mitochondrion. This is a ribosome-mediated process in which the information in messenger RNA (mRNA) is used to specify the sequence of amino acids in the protein; the mitochondrion has its own ribosomes and transfer RNAs, and uses a genetic code that differs from the nuclear code.
ribosomal small subunit assembly	The aggregation, arrangement and bonding together of constituent RNAs and proteins to form the small ribosomal subunit.
translation	The cellular metabolic process in which a protein is formed, using the sequence of a mature mRNA or circRNA molecule to specify the sequence of amino acids in a polypeptide chain. Translation is mediated by the ribosome, and begins with the formation of a ternary complex between aminoacylated initiator methionine tRNA, GTP, and initiation factor 2, which subsequently associates with the small subunit of the ribosome and an mRNA or circRNA. Translation ends with the release of a polypeptide chain from the ribosome.

4 homologous proteins in AiPD

UniProt AC	Gene Name	Protein Name	Species	Evidence Code
Q95H53	rps11	30S ribosomal protein S11, chloroplastic	Triticum aestivum (Wheat)	PR
P62263	RPS14	40S ribosomal protein S14	Homo sapiens (Human)	PR
P0C464	rps11	30S ribosomal protein S11, chloroplastic	Oryza sativa subsp japonica (Rice)	PR
A1E9V7	rps11	30S ribosomal protein S11, chloroplastic	Sorghum bicolor (Sorghum) (Sorghum vulgare)	PR

10	20	30	40	50	60
MQAVRNAGSR	FLRSWTWPQT	AGRVVARTPA	GTICTGARQL	QDAAAKQKVE	QNAAPSHTKF
70	80	90	100	110	120
SIYPPIPGEE	SSLRWAGKKF	EEIPIAHIKA	SHNNTQIQVV	SASNEPLAFA	SCGTEGFRNA
130	140	150	160	170	180
KKGTGIAAQT	AGIAAAARAK	QKGVIHIRVV	VKGLGPGRLS	AMHGLIMGGL	EVISITDNTP
190
IPHNGCRPRK	ARKL