Descriptions

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

Autoinhibitory domains (AIDs)

Target domain

Relief mechanism

Assay

cis-regPred

Accessory elements

No accessory elements

Autoinhibited structure

Activated structure

1 structures for Q56YN8

Entry ID Method Resolution Chain Position Source
AF-Q56YN8-F1 Predicted AlphaFoldDB

53 variants for Q56YN8

Variant ID(s) Position Change Description Diseaes Association Provenance
ENSVATH05603805 58 S>C No 1000Genomes
tmp_2_11616404_A_T 81 V>E No 1000Genomes
ENSVATH00250828 229 D>E No 1000Genomes
tmp_2_11615127_G_C 236 R>G No 1000Genomes
ENSVATH05603782 245 A>T No 1000Genomes
ENSVATH05603780 256 M>T No 1000Genomes
ENSVATH13428081 260 V>L No 1000Genomes
ENSVATH13428079 289 E>K No 1000Genomes
ENSVATH05603778 292 E>K No 1000Genomes
tmp_2_11614681_T_C 297 K>E No 1000Genomes
ENSVATH13428078 306 E>D No 1000Genomes
tmp_2_11614644_A_T 309 V>E No 1000Genomes
ENSVATH05603765 353 S>G No 1000Genomes
tmp_2_11614297_C_T 364 R>K No 1000Genomes
tmp_2_11613662_G_A 422 R>C No 1000Genomes
ENSVATH05603755 437 H>Y No 1000Genomes
tmp_2_11613607_T_C 440 E>G No 1000Genomes
tmp_2_11613580_G_A 449 S>F No 1000Genomes
ENSVATH05603753 482 E>Q No 1000Genomes
ENSVATH05603752 488 T>A No 1000Genomes
tmp_2_11612992_C_T 544 V>I No 1000Genomes
tmp_2_11612763_G_A 587 P>S No 1000Genomes
ENSVATH13428054 599 P>L No 1000Genomes
ENSVATH05603732 711 L>F No 1000Genomes
tmp_2_11611969_T_G 743 I>L No 1000Genomes
tmp_2_11611968_A_C 743 I>S No 1000Genomes
ENSVATH05603729 751 G>A No 1000Genomes
ENSVATH14559125 775 L>F No 1000Genomes
tmp_2_11611742_C_G 785 E>Q No 1000Genomes
tmp_2_11611691_A_T 802 F>I No 1000Genomes
ENSVATH13428023 834 Q>H No 1000Genomes
tmp_2_11611374_C_T 850 G>D No 1000Genomes
ENSVATH05603723 862 S>L No 1000Genomes
ENSVATH01906017 884 I>V No 1000Genomes
tmp_2_11611161_T_C 886 K>E No 1000Genomes
tmp_2_11611028_T_G 906 Q>H No 1000Genomes
tmp_2_11611026_T_C 907 D>G No 1000Genomes
ENSVATH00250824 917 S>T No 1000Genomes
ENSVATH13428017 919 R>H No 1000Genomes
ENSVATH14559112 921 T>M No 1000Genomes
tmp_2_11610689_A_T 951 N>K No 1000Genomes
ENSVATH05603711 951 N>T No 1000Genomes
ENSVATH13428002 959 L>V No 1000Genomes
tmp_2_11610420_C_T 1014 R>Q No 1000Genomes
tmp_2_11610369_C_T 1031 R>K No 1000Genomes
ENSVATH01906011 1055 N>H No 1000Genomes
ENSVATH05603695 1066 G>D No 1000Genomes
ENSVATH14559106 1086 S>T No 1000Genomes
tmp_2_11609652_T_A 1094 Q>H No 1000Genomes
tmp_2_11609483_C_T 1151 D>N No 1000Genomes
ENSVATH05603691 1152 Y>F No 1000Genomes
ENSVATH05603688 1169 A>T No 1000Genomes
ENSVATH05603686 1188 S>L No 1000Genomes

No associated diseases with Q56YN8

3 regional properties for Q56YN8

Type Name Position InterPro Accession
domain RecF/RecN/SMC, N-terminal 2 - 1180 IPR003395
domain SMCs flexible hinge 522 - 634 IPR010935
domain Structural maintenance of chromosomes 3, ABC domain, eukaryotic 3 - 166 IPR041741

Functions

Description
EC Number
Subcellular Localization
  • Nucleus
  • Cytoplasm
  • Nucleus matrix
  • Chromosome
  • Cytoplasm, cytoskeleton, spindle
  • Chromosome, centromere
  • Primarily associated with the nuclear matrix during interphase and with chromatin from prophase through anaphase in both somatic and meiotic cells
  • During mitosis and meiosis the protein also colocalized with the spindle from metaphase to telophase
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category No pathway information available

8 GO annotations of cellular component

Name Definition
chromatin The ordered and organized complex of DNA, protein, and sometimes RNA, that forms the chromosome.
chromosome, centromeric region The region of a chromosome that includes the centromeric DNA and associated proteins. In monocentric chromosomes, this region corresponds to a single area of the chromosome, whereas in holocentric chromosomes, it is evenly distributed along the chromosome.
cohesin complex A protein complex that is required for sister chromatid cohesion in eukaryotes. The cohesin complex forms a molecular ring complex, and is composed of structural maintenance of chromosomes (SMC) and kleisin proteins. For example, in yeast, the complex is composed of the SMC proteins Smc1p and Smc3p, and the kleisin protein Scc1p. In vertebrates, the complex is composed of the SMC1 (SMC1A or SMC1B) and SMC3 heterodimer attached via their hinge domains to a kleisin (RAD21, REC8 or RAD21L) which links them, and one STAG protein (STAG1, STAG2 or STAG3).
cytoplasm The contents of a cell excluding the plasma membrane and nucleus, but including other subcellular structures.
nuclear matrix The dense fibrillar network lying on the inner side of the nuclear membrane.
nucleus A membrane-bounded organelle of eukaryotic cells in which chromosomes are housed and replicated. In most cells, the nucleus contains all of the cell's chromosomes except the organellar chromosomes, and is the site of RNA synthesis and processing. In some species, or in specialized cell types, RNA metabolism or DNA replication may be absent.
plasmodesma A fine cytoplasmic channel, found in all higher plants, that connects the cytoplasm of one cell to that of an adjacent cell.
spindle The array of microtubules and associated molecules that forms between opposite poles of a eukaryotic cell during mitosis or meiosis and serves to move the duplicated chromosomes apart.

5 GO annotations of molecular function

Name Definition
ATP binding Binding to ATP, adenosine 5'-triphosphate, a universally important coenzyme and enzyme regulator.
ATP hydrolysis activity Catalysis of the reaction: ATP + H2O = ADP + H+ phosphate. ATP hydrolysis is used in some reactions as an energy source, for example to catalyze a reaction or drive transport against a concentration gradient.
chromatin binding Binding to chromatin, the network of fibers of DNA, protein, and sometimes RNA, that make up the chromosomes of the eukaryotic nucleus during interphase.
cohesin loading activity Facilitating a conformational change to load a cohesin complex around sister chromatids, driven by ATP hydrolysis.
double-stranded DNA binding Binding to double-stranded DNA.

6 GO annotations of biological process

Name Definition
cell division The process resulting in division and partitioning of components of a cell to form more cells; may or may not be accompanied by the physical separation of a cell into distinct, individually membrane-bounded daughter cells.
chromosome segregation The process in which genetic material, in the form of chromosomes, is organized into specific structures and then physically separated and apportioned to two or more sets. In eukaryotes, chromosome segregation begins with the condensation of chromosomes, includes chromosome separation, and ends when chromosomes have completed movement to the spindle poles.
DNA repair The process of restoring DNA after damage. Genomes are subject to damage by chemical and physical agents in the environment (e.g. UV and ionizing radiations, chemical mutagens, fungal and bacterial toxins, etc.) and by free radicals or alkylating agents endogenously generated in metabolism. DNA is also damaged because of errors during its replication. A variety of different DNA repair pathways have been reported that include direct reversal, base excision repair, nucleotide excision repair, photoreactivation, bypass, double-strand break repair pathway, and mismatch repair pathway.
meiotic cell cycle Progression through the phases of the meiotic cell cycle, in which canonically a cell replicates to produce four offspring with half the chromosomal content of the progenitor cell via two nuclear divisions.
mitotic sister chromatid cohesion The cell cycle process in which the sister chromatids of a replicated chromosome are joined along the entire length of the chromosome, from their formation in S phase through metaphase during a mitotic cell cycle. This cohesion cycle is critical for high fidelity chromosome transmission.
sister chromatid cohesion The cell cycle process in which the sister chromatids of a replicated chromosome become tethered to each other.

1 homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
Q9UQE7 SMC3 Structural maintenance of chromosomes protein 3 Homo sapiens (Human) PR
10 20 30 40 50 60
MFIKQVIIEG FKSYKEQVAT EEFSNKVNCV VGANGSGKSN FFHAIRFVLS DIYQNLRSED
70 80 90 100 110 120
RHALLHEGAG HQVVSAFVEI VFDNSDNRFP VDKEEIRLRR TVGLKKDDYF LDGKHITKGE
130 140 150 160 170 180
VMNLLESAGF SRANPYYVVQ QGKIASLTLM KDIERLDLLK EIGGTRVYEE RRRESLRIMQ
190 200 210 220 230 240
ETGNKRKQII EVVHYLDERL RELDEEKEEL RKYQQLDKQR KSLEYTIYDK ELHDAREKLE
250 260 270 280 290 300
QVEVARTKAS EESTKMYDRV EKAQDDSKSL DESLKELTKE LQTLYKEKET VEAQQTKALK
310 320 330 340 350 360
KKTKLELDVK DFQDRITGNI QSKNDALEQL NTVEREMQDS LRELEAIKPL YESQVDKENQ
370 380 390 400 410 420
TSKRINELEK TLSILYQKQG RATQFSNKAA RDKWLRKEIE DLKRVLDSNT VQEQKLQDEI
430 440 450 460 470 480
LRLNTDLTER DEHIKKHEVE IGELESRISK SHELFNTKKR ERDEEQRKRK EKWGEESQLS
490 500 510 520 530 540
SEIDKLKTEL ERAKKNLDHA TPGDVRRGLN SIRRICADYR INGVFGPLVE LVDCDEKFFT
550 560 570 580 590 600
AVEVTAGNSL FNVVVENDDI STKIIRHLNS LKGGRVTFLP LNRIKAPRVN YPKDSDAIPL
610 620 630 640 650 660
LKKLKFDSKF EPALGQVFGR TVVCRDLNVA TRVAKNDDLD CITMEGDQVS RKGGMTGGFY
670 680 690 700 710 720
DHRRSKLRFM NIIMQNTKSI NEKEKELEDV RRQLQVIDQQ ITQLVTEQQR LEADWTLCKL
730 740 750 760 770 780
QVEQLKQEIA NANKQKHAIH KAIEYKEKLL GDIRTRIDQV RSSMSMKEAE MGTELVDHLT
790 800 810 820 830 840
PEEREQLSKL NPEIKDLKEK KFAYQADRIE RETRKAELEA NIATNLKRRI TELQATIASI
850 860 870 880 890 900
DDDSLPSSAG TKEQELDDAK LSVNEAAKEL KSVCDSIDEK TKQIKKIKDE KAKLKTLEDD
910 920 930 940 950 960
CKGTLQDLDK KLEELFSLRN TLLAKQDEYT KKIRGLGPLS SDAFDTYKRK NIKELQKMLH
970 980 990 1000 1010 1020
RCSEQLQQFS HVNKKALDQY VNFTEQREEL QNRQAELDAG DEKIKELITV LDQRKDESIE
1030 1040 1050 1060 1070 1080
RTFKGVAHHF RDVFSELVQD GYGNLIIMKK KDLDNDDEDD DDDDGGREAV TEGRVEKYIG
1090 1100 1110 1120 1130 1140
VKVKVSFTGQ GETQLMKQLS GGQKTVVALA LIFAIQRCDP APFYLFDEID AALDPQYRTA
1150 1160 1170 1180 1190 1200
VGNLIRRLAD DYGTQFITTT FRPELVRVAD KIYGVFHKNR VSIVNVISKD QALDFIEKDQ
SHDT