DNA replication, replication factor A, 51kDa subunit RPA1
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 4 |
Pissara et al. | yes | yes: 20 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 6 |
GO:0043226 | organelle | 2 | 6 |
GO:0043227 | membrane-bounded organelle | 3 | 6 |
GO:0043229 | intracellular organelle | 3 | 6 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005662 | DNA replication factor A complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0034399 | nuclear periphery | 2 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4I3Q8
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006259 | DNA metabolic process | 4 | 7 |
GO:0006260 | DNA replication | 5 | 6 |
GO:0006281 | DNA repair | 5 | 7 |
GO:0006310 | DNA recombination | 5 | 7 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0006950 | response to stress | 2 | 7 |
GO:0006974 | DNA damage response | 4 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0033554 | cellular response to stress | 3 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0050896 | response to stimulus | 1 | 7 |
GO:0051716 | cellular response to stimulus | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
GO:0000723 | telomere maintenance | 5 | 1 |
GO:0000724 | double-strand break repair via homologous recombination | 7 | 1 |
GO:0000725 | recombinational repair | 6 | 1 |
GO:0006268 | DNA unwinding involved in DNA replication | 9 | 1 |
GO:0006278 | RNA-templated DNA biosynthetic process | 6 | 1 |
GO:0006289 | nucleotide-excision repair | 6 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007004 | telomere maintenance via telomerase | 7 | 1 |
GO:0007049 | cell cycle | 2 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0010833 | telomere maintenance via telomere lengthening | 6 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0022414 | reproductive process | 1 | 1 |
GO:0032200 | telomere organization | 6 | 1 |
GO:0032392 | DNA geometric change | 7 | 1 |
GO:0032508 | DNA duplex unwinding | 8 | 1 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0051321 | meiotic cell cycle | 2 | 1 |
GO:0071103 | DNA conformation change | 6 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0071897 | DNA biosynthetic process | 5 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 7 |
GO:0003677 | DNA binding | 4 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0003684 | damaged DNA binding | 5 | 1 |
GO:0003697 | single-stranded DNA binding | 5 | 1 |
GO:0042162 | telomeric DNA binding | 6 | 1 |
GO:0043047 | single-stranded telomeric DNA binding | 7 | 1 |
GO:0043565 | sequence-specific DNA binding | 5 | 1 |
GO:0098847 | sequence-specific single stranded DNA binding | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.294 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.359 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.359 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.294 |
CLV_PCSK_PC1ET2_1 | 172 | 174 | PF00082 | 0.359 |
CLV_PCSK_PC1ET2_1 | 379 | 381 | PF00082 | 0.359 |
CLV_PCSK_PC7_1 | 168 | 174 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.461 |
CLV_Separin_Metazoa | 458 | 462 | PF03568 | 0.578 |
DEG_APCC_DBOX_1 | 273 | 281 | PF00400 | 0.469 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.643 |
DOC_MAPK_gen_1 | 287 | 296 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 396 | 405 | PF00069 | 0.359 |
DOC_MAPK_gen_1 | 423 | 431 | PF00069 | 0.359 |
DOC_MAPK_MEF2A_6 | 128 | 136 | PF00069 | 0.436 |
DOC_MAPK_MEF2A_6 | 344 | 351 | PF00069 | 0.359 |
DOC_MAPK_MEF2A_6 | 399 | 407 | PF00069 | 0.359 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.567 |
DOC_USP7_UBL2_3 | 172 | 176 | PF12436 | 0.359 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.461 |
LIG_14-3-3_CanoR_1 | 108 | 114 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 26 | 35 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 423 | 429 | PF00244 | 0.359 |
LIG_14-3-3_CanoR_1 | 430 | 437 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 60 | 64 | PF00244 | 0.494 |
LIG_Actin_WH2_2 | 196 | 212 | PF00022 | 0.359 |
LIG_APCC_ABBA_1 | 360 | 365 | PF00400 | 0.359 |
LIG_APCC_ABBAyCdc20_2 | 60 | 66 | PF00400 | 0.494 |
LIG_BIR_III_2 | 311 | 315 | PF00653 | 0.359 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.493 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.440 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.359 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.454 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.351 |
LIG_FHA_2 | 164 | 170 | PF00498 | 0.359 |
LIG_FHA_2 | 223 | 229 | PF00498 | 0.317 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.359 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.560 |
LIG_FHA_2 | 452 | 458 | PF00498 | 0.399 |
LIG_FHA_2 | 49 | 55 | PF00498 | 0.494 |
LIG_GBD_Chelix_1 | 145 | 153 | PF00786 | 0.359 |
LIG_LIR_Apic_2 | 37 | 41 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 292 | 301 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 356 | 366 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 49 | 58 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 213 | 217 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 292 | 296 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 356 | 362 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 432 | 437 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 49 | 53 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 69 | 74 | PF02991 | 0.331 |
LIG_PCNA_yPIPBox_3 | 138 | 146 | PF02747 | 0.359 |
LIG_Pex14_1 | 359 | 363 | PF04695 | 0.359 |
LIG_SH2_CRK | 129 | 133 | PF00017 | 0.433 |
LIG_SH2_PTP2 | 293 | 296 | PF00017 | 0.359 |
LIG_SH2_SRC | 293 | 296 | PF00017 | 0.359 |
LIG_SH2_STAP1 | 102 | 106 | PF00017 | 0.494 |
LIG_SH2_STAT3 | 302 | 305 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.494 |
LIG_SH3_4 | 40 | 47 | PF00018 | 0.494 |
LIG_SUMO_SIM_anti_2 | 144 | 150 | PF11976 | 0.359 |
LIG_TRAF2_1 | 417 | 420 | PF00917 | 0.323 |
LIG_TRAF2_1 | 440 | 443 | PF00917 | 0.527 |
LIG_WRC_WIRS_1 | 211 | 216 | PF05994 | 0.359 |
LIG_WRC_WIRS_1 | 47 | 52 | PF05994 | 0.494 |
LIG_WRC_WIRS_1 | 68 | 73 | PF05994 | 0.474 |
MOD_CDK_SPxxK_3 | 337 | 344 | PF00069 | 0.461 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.359 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.479 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.550 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.359 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.323 |
MOD_CK2_1 | 437 | 443 | PF00069 | 0.548 |
MOD_Cter_Amidation | 272 | 275 | PF01082 | 0.485 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.577 |
MOD_GlcNHglycan | 54 | 58 | PF01048 | 0.294 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.294 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.552 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.359 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.359 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.414 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.417 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.494 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.303 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.294 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.359 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.564 |
MOD_N-GLC_1 | 250 | 255 | PF02516 | 0.544 |
MOD_N-GLC_1 | 353 | 358 | PF02516 | 0.359 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.355 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.359 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.452 |
MOD_NEK2_2 | 358 | 363 | PF00069 | 0.461 |
MOD_PIKK_1 | 159 | 165 | PF00454 | 0.335 |
MOD_PIKK_1 | 254 | 260 | PF00454 | 0.531 |
MOD_PIKK_1 | 339 | 345 | PF00454 | 0.359 |
MOD_PIKK_1 | 353 | 359 | PF00454 | 0.359 |
MOD_PIKK_1 | 40 | 46 | PF00454 | 0.494 |
MOD_PKA_1 | 318 | 324 | PF00069 | 0.359 |
MOD_PKA_1 | 93 | 99 | PF00069 | 0.494 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.457 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.567 |
MOD_PKA_2 | 424 | 430 | PF00069 | 0.355 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.494 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.494 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.534 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.332 |
MOD_Plk_1 | 184 | 190 | PF00069 | 0.359 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.538 |
MOD_Plk_1 | 335 | 341 | PF00069 | 0.348 |
MOD_Plk_2-3 | 141 | 147 | PF00069 | 0.359 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.359 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.359 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.359 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.452 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.315 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.359 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.494 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.441 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.461 |
MOD_SUMO_for_1 | 289 | 292 | PF00179 | 0.474 |
MOD_SUMO_for_1 | 407 | 410 | PF00179 | 0.359 |
MOD_SUMO_rev_2 | 191 | 195 | PF00179 | 0.337 |
MOD_SUMO_rev_2 | 233 | 240 | PF00179 | 0.467 |
TRG_DiLeu_BaEn_1 | 141 | 146 | PF01217 | 0.359 |
TRG_DiLeu_BaEn_1 | 458 | 463 | PF01217 | 0.577 |
TRG_DiLeu_BaEn_4 | 419 | 425 | PF01217 | 0.359 |
TRG_DiLeu_BaLyEn_6 | 70 | 75 | PF01217 | 0.567 |
TRG_DiLeu_LyEn_5 | 458 | 463 | PF01217 | 0.577 |
TRG_ENDOCYTIC_2 | 129 | 132 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.344 |
TRG_ER_diArg_1 | 25 | 28 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 403 | 406 | PF00400 | 0.303 |
TRG_ER_diArg_1 | 423 | 426 | PF00400 | 0.131 |
TRG_ER_diArg_1 | 445 | 447 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 93 | 95 | PF00400 | 0.494 |
TRG_NLS_MonoExtC_3 | 378 | 384 | PF00514 | 0.359 |
TRG_Pf-PMV_PEXEL_1 | 275 | 279 | PF00026 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 287 | 292 | PF00026 | 0.582 |
TRG_Pf-PMV_PEXEL_1 | 446 | 450 | PF00026 | 0.649 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P825 | Leptomonas seymouri | 93% | 100% |
A0A0S4J8L0 | Bodo saltans | 56% | 97% |
A0A1X0NQV3 | Trypanosomatidae | 69% | 99% |
A0A3R7KN38 | Trypanosoma rangeli | 73% | 100% |
A0A3S7X1P8 | Leishmania donovani | 100% | 100% |
A4HGN5 | Leishmania braziliensis | 98% | 100% |
D0A8A0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 68% | 100% |
D8UYN9 | Tetrahymena thermophila (strain SB210) | 25% | 70% |
E9B001 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 99% | 100% |
O97472 | Caenorhabditis briggsae | 29% | 71% |
P22336 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 75% |
P27694 | Homo sapiens | 35% | 76% |
Q01588 | Xenopus laevis | 33% | 77% |
Q10Q08 | Oryza sativa subsp. japonica | 35% | 74% |
Q19537 | Caenorhabditis elegans | 29% | 71% |
Q23696 | Crithidia fasciculata | 92% | 100% |
Q24492 | Drosophila melanogaster | 35% | 77% |
Q4Q884 | Leishmania major | 99% | 100% |
Q5FW17 | Xenopus tropicalis | 33% | 77% |
Q5R7Q4 | Pongo abelii | 35% | 76% |
Q5ZJJ2 | Gallus gallus | 34% | 76% |
Q6NY74 | Danio rerio | 34% | 78% |
Q6YZ49 | Oryza sativa subsp. japonica | 33% | 71% |
Q8VEE4 | Mus musculus | 34% | 75% |
Q92372 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 77% |
Q9FME0 | Arabidopsis thaliana | 33% | 74% |
Q9SD82 | Arabidopsis thaliana | 35% | 77% |
Q9SKI4 | Arabidopsis thaliana | 32% | 73% |
V5DBB0 | Trypanosoma cruzi | 74% | 100% |