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 Q9SMV7

Entry ID Method Resolution Chain Position Source
AF-Q9SMV7-F1 Predicted AlphaFoldDB

95 variants for Q9SMV7

Variant ID(s) Position Change Description Diseaes Association Provenance
ENSVATH10944674 14 P>T No 1000Genomes
tmp_3_8918041_C_T 16 A>T No 1000Genomes
ENSVATH02193855 20 K>E No 1000Genomes
ENSVATH05904416 27 A>V No 1000Genomes
tmp_3_8917999_C_A 30 G>C No 1000Genomes
tmp_3_8917969_T_G 40 N>H No 1000Genomes
ENSVATH10944671 52 V>L No 1000Genomes
tmp_3_8917913_T_A 58 K>N No 1000Genomes
ENSVATH00345559 62 E>D No 1000Genomes
ENSVATH02193854 79 P>T No 1000Genomes
ENSVATH10944670 85 A>P No 1000Genomes
tmp_3_8917827_G_A 87 S>F No 1000Genomes
tmp_3_8917821_C_G 89 G>A No 1000Genomes
tmp_3_8917818_T_A 90 D>V No 1000Genomes
tmp_3_8917816_C_T 91 A>T No 1000Genomes
ENSVATH10944669 92 S>L No 1000Genomes
ENSVATH05904414 105 V>D No 1000Genomes
ENSVATH05904413 110 C>Y No 1000Genomes
tmp_3_8917753_C_T 112 G>R No 1000Genomes
tmp_3_8917602_G_A 121 P>L No 1000Genomes
tmp_3_8917532_T_G 144 K>N No 1000Genomes
ENSVATH00345558 170 G>D No 1000Genomes
ENSVATH10944668 177 T>I No 1000Genomes
tmp_3_8917398_C_A 189 R>L No 1000Genomes
ENSVATH10944667 197 F>L No 1000Genomes
ENSVATH05904408 217 P>L No 1000Genomes
tmp_3_8917296_T_G 223 K>T No 1000Genomes
tmp_3_8917285_C_G 227 E>Q No 1000Genomes
tmp_3_8917281_C_T 228 G>E No 1000Genomes
tmp_3_8917255_A_T 237 S>T No 1000Genomes
tmp_3_8917225_G_A 247 P>S No 1000Genomes
ENSVATH10944666 255 K>N No 1000Genomes
tmp_3_8917111_C_T 285 V>M No 1000Genomes
tmp_3_8916140_G_A 378 A>V No 1000Genomes
tmp_3_8916091_T_G 394 K>N No 1000Genomes
tmp_3_8915632_T_A 397 K>N No 1000Genomes
ENSVATH02193843 398 M>I No 1000Genomes
ENSVATH10944615 421 V>I No 1000Genomes
ENSVATH05904395 439 Q>H No 1000Genomes
ENSVATH10944602 449 S>G No 1000Genomes
ENSVATH10944601 463 Y>F No 1000Genomes
tmp_3_8915233_G_A 464 T>M No 1000Genomes
tmp_3_8915100_C_G 474 A>P No 1000Genomes
ENSVATH10944598 478 Q>H No 1000Genomes
ENSVATH10944597 481 G>R No 1000Genomes
ENSVATH00345546 502 S>F No 1000Genomes
ENSVATH05904389 505 W>L No 1000Genomes
ENSVATH05904390 505 W>R No 1000Genomes
tmp_3_8915000_C_A 507 C>F No 1000Genomes
ENSVATH02193839 519 L>H No 1000Genomes
ENSVATH13993504 533 K>Q No 1000Genomes
tmp_3_8914820_G_T 540 H>N No 1000Genomes
tmp_3_8914811_T_A 543 I>F No 1000Genomes
ENSVATH10944595 570 C>S No 1000Genomes
ENSVATH02193837 649 V>I No 1000Genomes
ENSVATH00345545 650 R>Q No 1000Genomes
tmp_3_8914357_A_G 655 V>A No 1000Genomes
ENSVATH00345544 655 V>L No 1000Genomes
tmp_3_8914130_T_C 683 I>V No 1000Genomes
tmp_3_8914104_C_A 691 K>N No 1000Genomes
tmp_3_8914105_T_G 691 K>T No 1000Genomes
tmp_3_8914079_A_T 700 Y>N No 1000Genomes
ENSVATH00345543 715 E>Q No 1000Genomes
ENSVATH05904381 727 S>G No 1000Genomes
tmp_3_8913995_C_T 728 D>N No 1000Genomes
ENSVATH00345542 732 Y>C No 1000Genomes
ENSVATH00345542 732 Y>F No 1000Genomes
tmp_3_8913798_T_G 735 Q>H No 1000Genomes
ENSVATH00345541 736 D>E No 1000Genomes
tmp_3_8913797_C_T 736 D>N No 1000Genomes
ENSVATH13993500 741 N>K No 1000Genomes
tmp_3_8913758_T_C 749 I>V No 1000Genomes
tmp_3_8913743_C_T 754 E>K No 1000Genomes
ENSVATH10944547 783 A>D No 1000Genomes
ENSVATH02193831 787 A>V No 1000Genomes
tmp_3_8913638_G_C 789 P>A No 1000Genomes
tmp_3_8913518_G_A 829 P>S No 1000Genomes
tmp_3_8913281_G_A 880 P>L No 1000Genomes
tmp_3_8913278_C_G 881 C>S No 1000Genomes
ENSVATH00345538 886 I>M No 1000Genomes
tmp_3_8913093_G_A 914 T>I No 1000Genomes
tmp_3_8912821_G_A 976 A>V No 1000Genomes
tmp_3_8912809_C_T 980 R>H No 1000Genomes
tmp_3_8912807_C_G 981 V>L No 1000Genomes
ENSVATH10944521 983 S>L No 1000Genomes
tmp_3_8912770_C_T 993 R>K No 1000Genomes
ENSVATH05904374 999 R>G No 1000Genomes
tmp_3_8912738_C_T 1004 D>N No 1000Genomes
tmp_3_8912711_C_T 1013 E>K No 1000Genomes
ENSVATH05904373 1040 G>V No 1000Genomes
ENSVATH10944518 1084 A>T No 1000Genomes
ENSVATH05904370 1084 A>V No 1000Genomes
ENSVATH13993496 1091 Y>S No 1000Genomes
tmp_3_8912474_C_T 1092 D>N No 1000Genomes
ENSVATH10944517 1102 K>R No 1000Genomes

No associated diseases with Q9SMV7

4 regional properties for Q9SMV7

Type Name Position InterPro Accession
domain DNA mismatch repair protein MutS, C-terminal 846 - 1045 IPR000432
domain DNA mismatch repair protein MutS-like, N-terminal 270 - 380 IPR007695
domain DNA mismatch repair protein MutS, core 558 - 822 IPR007696
domain DNA mismatch repair protein MutS, connector domain 390 - 540 IPR007860

Functions

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

2 GO annotations of cellular component

Name Definition
MutSalpha complex A heterodimer involved in the recognition and repair of base-base and small insertion/deletion mismatches. In human the complex consists of two subunits, MSH2 and MSH6.
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.

4 GO annotations of molecular function

Name Definition
ATP binding Binding to ATP, adenosine 5'-triphosphate, a universally important coenzyme and enzyme regulator.
ATP-dependent DNA damage sensor activity A molecule that recognises toxic DNA structures, and initiates a signalling response, driven by ATP hydrolysis.
double-stranded DNA binding Binding to double-stranded DNA.
mismatched DNA binding Binding to a double-stranded DNA region containing one or more mismatches.

1 GO annotations of biological process

Name Definition
mismatch repair A system for the correction of errors in which an incorrect base, which cannot form hydrogen bonds with the corresponding base in the parent strand, is incorporated into the daughter strand. The mismatch repair system promotes genomic fidelity by repairing base-base mismatches, insertion-deletion loops and heterologies generated during DNA replication and recombination.

3 homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
P52701 MSH6 DNA mismatch repair protein Msh6 Homo sapiens (Human) PR
F4JP48 MSH4 DNA mismatch repair protein MSH4 Arabidopsis thaliana (Mouse-ear cress) PR
O04716 MSH6 DNA mismatch repair protein MSH6 Arabidopsis thaliana (Mouse-ear cress) PR
10 20 30 40 50 60
MQRQRSILSF FQKPTAATTK GLVSGDAASG GGGSGGPRFN VKEGDAKGDA SVRFAVSKSV
70 80 90 100 110 120
DEVRGTDTPP EKVPRRVLPS GFKPAESAGD ASSLFSNIMH KFVKVDDRDC SGERSREDVV
130 140 150 160 170 180
PLNDSSLCMK ANDVIPQFRS NNGKTQERNH AFSFSGRAEL RSVEDIGVDG DVPGPETPGM
190 200 210 220 230 240
RPRASRLKRV LEDEMTFKED KVPVLDSNKR LKMLQDPVCG EKKEVNEGTK FEWLESSRIR
250 260 270 280 290 300
DANRRRPDDP LYDRKTLHIP PDVFKKMSAS QKQYWSVKSE YMDIVLFFKV GKFYELYELD
310 320 330 340 350 360
AELGHKELDW KMTMSGVGKC RQVGISESGI DEAVQKLLAR GYKVGRIEQL ETSDQAKARG
370 380 390 400 410 420
ANTIIPRKLV QVLTPSTASE GNIGPDAVHL LAIKEIKMEL QKCSTVYGFA FVDCAALRFW
430 440 450 460 470 480
VGSISDDASC AALGALLMQV SPKEVLYDSK GLSREAQKAL RKYTLTGSTA VQLAPVPQVM
490 500 510 520 530 540
GDTDAAGVRN IIESNGYFKG SSESWNCAVD GLNECDVALS ALGELINHLS RLKLEDVLKH
550 560 570 580 590 600
GDIFPYQVYR GCLRIDGQTM VNLEIFNNSC DGGPSGTLYK YLDNCVSPTG KRLLRNWICH
610 620 630 640 650 660
PLKDVESINK RLDVVEEFTA NSESMQITGQ YLHKLPDLER LLGRIKSSVR SSASVLPALL
670 680 690 700 710 720
GKKVLKQRVK AFGQIVKGFR SGIDLLLALQ KESNMMSLLY KLCKLPILVG KSGLELFLSQ
730 740 750 760 770 780
FEAAIDSDFP NYQNQDVTDE NAETLTILIE LFIERATQWS EVIHTISCLD VLRSFAIAAS
790 800 810 820 830 840
LSAGSMARPV IFPESEATDQ NQKTKGPILK IQGLWHPFAV AADGQLPVPN DILLGEARRS
850 860 870 880 890 900
SGSIHPRSLL LTGPNMGGKS TLLRATCLAV IFAQLGCYVP CESCEISLVD TIFTRLGASD
910 920 930 940 950 960
RIMTGESTFL VECTETASVL QNATQDSLVI LDELGRGTST FDGYAIAYSV FRHLVEKVQC
970 980 990 1000 1010 1020
RMLFATHYHP LTKEFASHPR VTSKHMACAF KSRSDYQPRG CDQDLVFLYR LTEGACPESY
1030 1040 1050 1060 1070 1080
GLQVALMAGI PNQVVETASG AAQAMKRSIG ENFKSSELRS EFSSLHEDWL KSLVGISRVA
1090 1100
HNNAPIGEDD YDTLFCLWHE IKSSYCVPK