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 Q9Z7G7

Entry ID Method Resolution Chain Position Source
AF-Q9Z7G7-F1 Predicted AlphaFoldDB

No variants for Q9Z7G7

Variant ID(s) Position Change Description Diseaes Association Provenance
No variants for Q9Z7G7

No associated diseases with Q9Z7G7

2 regional properties for Q9Z7G7

Type Name Position InterPro Accession
domain UvrD-like helicase, ATP-binding domain 1 - 443 IPR014016
domain UvrD-like DNA helicase, C-terminal 643 - 742 IPR014017

Functions

Description
EC Number 3.1.11.5 Exodeoxyribonucleases producing 5'-phosphomonoesters
Subcellular Localization
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category No pathway information available

No GO annotations of cellular component

Name Definition
No GO annotations for cellular component

5 GO annotations of molecular function

Name Definition
ATP binding Binding to ATP, adenosine 5'-triphosphate, a universally important coenzyme and enzyme regulator.
DNA binding Any molecular function by which a gene product interacts selectively and non-covalently with DNA (deoxyribonucleic acid).
DNA helicase activity Unwinding of a DNA helix, driven by ATP hydrolysis.
exodeoxyribonuclease V activity Catalysis of the exonucleolytic cleavage (in the presence of ATP) in either 5' to 3' or 3' to 5' direction to yield 5'-phosphooligonucleotides.
metal ion binding Binding to a metal ion.

1 GO annotations of biological process

Name Definition
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.

No homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
No homologous proteins
10 20 30 40 50 60
MKPFNIFDSN SSIQGKFFLE ASAGTGKTFT IEQIVLRALI EGSLTHVEHA LAITFTNAST
70 80 90 100 110 120
NELKVRIKDN LAQTLRELKA VLNSQPASLP TYLDINCNVK QIYMQVRNAL ATLDQMSLFT
130 140 150 160 170 180
IHGFCNFVLE QYFPKTRLIH KNPALTHSQL VLHHITNYLK QDLWKNVLFQ EQFHLLAVRY
190 200 210 220 230 240
NVTSKHTSSL VDKLLASYTQ PISSYFSSRV ERLEQISLWH QQIYNSLLEI PKQVFLDQLT
250 260 270 280 290 300
AHISGFKKQP FSILDDLHHF VDLLYTSETH SSLFSFFKIA ETFNFKHRLA RYKPCAAFTV
310 320 330 340 350 360
LENMSWVERT LEFCNLDRIF NTLLVDLQEY LKQNYTPWLS PDESVFALEK LLSSSEAQPV
370 380 390 400 410 420
VQALREQYQL VLIDEFQDTD KQQWSIFSNL FISPKFTGSL FLIGDPKQSI YEWRSADLPT
430 440 450 460 470 480
YLTAKSSFSE DKQLQLVNNY RSTPKLMEAI NQIFGKISPF LEIPGYLPIE YHALNPQSSE
490 500 510 520 530 540
TFENPPHAPI HFFFYETIKD QALWIFSEAL RLQKEQKIPL GNMVVLVSDS NQAFELISYA
550 560 570 580 590 600
TIPVSFSKNK SIFHLTETHI LTTALLEAIL HPENYEKISK ILFSSLFGLS LDEVTTKKED
610 620 630 640 650 660
FTIYFQSLHS YISHHGLLAT FYRVMTTQGN VLFSSPRGDL IFQEMEKLCG YLDTISSYPY
670 680 690 700 710 720
HQLLHLKNFS ETGRWEEELA ISSYSEDLET LKITTIHSSK GLEYDIVFCP GIEKSKKNKS
730 740 750 760 770 780
SSELLREMYV ACTRAKKQLY LPISTQPPSL QRSSALTNYV KLEGTQSSAY DLAIHLHQEH
790 800 810 820 830 840
PDLFSYSLPK DHGHATTVLN LPLLETFALK VTPPKTIFSF SSTKFLLDTH KDSQSIPYSK
850 860 870 880 890 900
LPISKQQLPL GEKTGILIHK ILESIQFSLL QDTEYLMSTI MRFIKHTHLE GFEETILKLL
910 920 930 940 950 960
SKTFFSPLTF SSQTFSLSQV LPNKIFRETS FLFLENQELW QGVIDLFFEH EGKYYIIDWK
970 980 990 1000 1010 1020
TSFLGETNSD YSKSNLSIYI KQEKLDYQGR IYVKAVRKFL NQFEIDDDVE LGVIFIRGID
1030 1040
TQGNGFFALN SSEDIPNFNP KAIQKCQAYH