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: 0 |
Pissara et al. | no | yes: 0 |
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0008622 | epsilon DNA polymerase complex | 3 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0042575 | DNA polymerase complex | 3 | 12 |
GO:0061695 | transferase complex, transferring phosphorus-containing groups | 4 | 12 |
GO:0140513 | nuclear protein-containing complex | 2 | 12 |
GO:0140535 | intracellular protein-containing complex | 2 | 12 |
GO:1902494 | catalytic complex | 2 | 12 |
GO:1990234 | transferase complex | 3 | 12 |
Related structures:
AlphaFold database: A4HMK0
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006260 | DNA replication | 5 | 12 |
GO:0006261 | DNA-templated DNA replication | 6 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0000731 | DNA synthesis involved in DNA repair | 6 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006301 | postreplication repair | 6 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0019985 | translesion synthesis | 7 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 1 |
GO:0042276 | error-prone translesion synthesis | 8 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 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 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0005488 | binding | 1 | 12 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 8 |
GO:0016779 | nucleotidyltransferase activity | 4 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 165 | 169 | PF00656 | 0.372 |
CLV_C14_Caspase3-7 | 446 | 450 | PF00656 | 0.410 |
CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.278 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 423 | 425 | PF00675 | 0.245 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.302 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.358 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.256 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 473 | 477 | PF00082 | 0.294 |
DEG_APCC_DBOX_1 | 41 | 49 | PF00400 | 0.322 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.532 |
DEG_SPOP_SBC_1 | 112 | 116 | PF00917 | 0.469 |
DOC_CKS1_1 | 384 | 389 | PF01111 | 0.390 |
DOC_CKS1_1 | 538 | 543 | PF01111 | 0.298 |
DOC_CYCLIN_yClb1_LxF_4 | 409 | 414 | PF00134 | 0.245 |
DOC_CYCLIN_yCln2_LP_2 | 497 | 503 | PF00134 | 0.338 |
DOC_MAPK_DCC_7 | 16 | 24 | PF00069 | 0.378 |
DOC_MAPK_gen_1 | 192 | 199 | PF00069 | 0.383 |
DOC_MAPK_gen_1 | 270 | 279 | PF00069 | 0.459 |
DOC_MAPK_HePTP_8 | 489 | 501 | PF00069 | 0.309 |
DOC_MAPK_MEF2A_6 | 192 | 199 | PF00069 | 0.370 |
DOC_MAPK_MEF2A_6 | 272 | 280 | PF00069 | 0.449 |
DOC_MAPK_MEF2A_6 | 492 | 501 | PF00069 | 0.282 |
DOC_PIKK_1 | 183 | 191 | PF02985 | 0.382 |
DOC_PIKK_1 | 58 | 65 | PF02985 | 0.413 |
DOC_PP1_RVXF_1 | 194 | 200 | PF00149 | 0.370 |
DOC_PP1_RVXF_1 | 308 | 315 | PF00149 | 0.364 |
DOC_PP1_RVXF_1 | 409 | 415 | PF00149 | 0.268 |
DOC_PP2B_LxvP_1 | 497 | 500 | PF13499 | 0.265 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.419 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.316 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.522 |
DOC_USP7_UBL2_3 | 16 | 20 | PF12436 | 0.386 |
DOC_USP7_UBL2_3 | 194 | 198 | PF12436 | 0.236 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.390 |
DOC_WW_Pin1_4 | 479 | 484 | PF00397 | 0.390 |
DOC_WW_Pin1_4 | 537 | 542 | PF00397 | 0.285 |
LIG_14-3-3_CanoR_1 | 111 | 119 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 204 | 211 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 272 | 277 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 413 | 421 | PF00244 | 0.253 |
LIG_14-3-3_CanoR_1 | 470 | 476 | PF00244 | 0.414 |
LIG_Actin_WH2_2 | 184 | 200 | PF00022 | 0.374 |
LIG_Actin_WH2_2 | 294 | 312 | PF00022 | 0.397 |
LIG_BIR_III_2 | 449 | 453 | PF00653 | 0.167 |
LIG_BIR_III_2 | 96 | 100 | PF00653 | 0.237 |
LIG_eIF4E_1 | 364 | 370 | PF01652 | 0.167 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.394 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.320 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.202 |
LIG_FHA_1 | 470 | 476 | PF00498 | 0.400 |
LIG_FHA_1 | 503 | 509 | PF00498 | 0.378 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.341 |
LIG_FHA_2 | 464 | 470 | PF00498 | 0.271 |
LIG_FHA_2 | 472 | 478 | PF00498 | 0.217 |
LIG_FHA_2 | 538 | 544 | PF00498 | 0.298 |
LIG_LIR_Apic_2 | 535 | 541 | PF02991 | 0.293 |
LIG_LIR_Gen_1 | 10 | 19 | PF02991 | 0.284 |
LIG_LIR_Gen_1 | 226 | 235 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 25 | 34 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 317 | 327 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 365 | 373 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 466 | 476 | PF02991 | 0.258 |
LIG_LIR_Gen_1 | 47 | 54 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 10 | 14 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 226 | 230 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 25 | 30 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 317 | 323 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 365 | 370 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 466 | 471 | PF02991 | 0.258 |
LIG_LIR_Nem_3 | 47 | 52 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 516 | 522 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 535 | 539 | PF02991 | 0.188 |
LIG_PCNA_PIPBox_1 | 216 | 225 | PF02747 | 0.302 |
LIG_PCNA_PIPBox_1 | 291 | 300 | PF02747 | 0.390 |
LIG_PCNA_PIPBox_1 | 385 | 394 | PF02747 | 0.273 |
LIG_PCNA_yPIPBox_3 | 172 | 182 | PF02747 | 0.350 |
LIG_Pex14_1 | 223 | 227 | PF04695 | 0.228 |
LIG_Pex14_1 | 515 | 519 | PF04695 | 0.319 |
LIG_Pex14_2 | 316 | 320 | PF04695 | 0.387 |
LIG_Pex14_2 | 426 | 430 | PF04695 | 0.273 |
LIG_REV1ctd_RIR_1 | 295 | 304 | PF16727 | 0.245 |
LIG_SH2_CRK | 519 | 523 | PF00017 | 0.348 |
LIG_SH2_NCK_1 | 539 | 543 | PF00017 | 0.329 |
LIG_SH2_STAP1 | 364 | 368 | PF00017 | 0.167 |
LIG_SH2_STAT5 | 539 | 542 | PF00017 | 0.281 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.293 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.430 |
LIG_SH3_3 | 256 | 262 | PF00018 | 0.491 |
LIG_SH3_3 | 353 | 359 | PF00018 | 0.254 |
LIG_SH3_3 | 365 | 371 | PF00018 | 0.243 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.239 |
LIG_SH3_3 | 497 | 503 | PF00018 | 0.304 |
LIG_SH3_3 | 521 | 527 | PF00018 | 0.344 |
LIG_SUMO_SIM_anti_2 | 155 | 162 | PF11976 | 0.450 |
LIG_SUMO_SIM_anti_2 | 275 | 281 | PF11976 | 0.304 |
LIG_SUMO_SIM_par_1 | 155 | 162 | PF11976 | 0.248 |
LIG_SUMO_SIM_par_1 | 177 | 185 | PF11976 | 0.503 |
LIG_SUMO_SIM_par_1 | 20 | 25 | PF11976 | 0.373 |
LIG_SUMO_SIM_par_1 | 68 | 75 | PF11976 | 0.464 |
LIG_SUMO_SIM_par_1 | 91 | 96 | PF11976 | 0.274 |
LIG_TRAF2_1 | 72 | 75 | PF00917 | 0.385 |
LIG_TRFH_1 | 17 | 21 | PF08558 | 0.335 |
LIG_TRFH_1 | 255 | 259 | PF08558 | 0.408 |
LIG_TRFH_1 | 367 | 371 | PF08558 | 0.338 |
LIG_WRC_WIRS_1 | 224 | 229 | PF05994 | 0.226 |
LIG_WRC_WIRS_1 | 8 | 13 | PF05994 | 0.486 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.549 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.435 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.434 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.447 |
MOD_CK2_1 | 455 | 461 | PF00069 | 0.372 |
MOD_CK2_1 | 463 | 469 | PF00069 | 0.295 |
MOD_CK2_1 | 481 | 487 | PF00069 | 0.304 |
MOD_CK2_1 | 546 | 552 | PF00069 | 0.299 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.460 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.460 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.427 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.372 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.314 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.329 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.332 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.268 |
MOD_PIKK_1 | 203 | 209 | PF00454 | 0.287 |
MOD_PK_1 | 272 | 278 | PF00069 | 0.368 |
MOD_PKA_1 | 401 | 407 | PF00069 | 0.390 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.364 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.309 |
MOD_PKB_1 | 270 | 278 | PF00069 | 0.242 |
MOD_PKB_1 | 411 | 419 | PF00069 | 0.245 |
MOD_PKB_1 | 443 | 451 | PF00069 | 0.167 |
MOD_Plk_1 | 200 | 206 | PF00069 | 0.405 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.364 |
MOD_Plk_1 | 268 | 274 | PF00069 | 0.324 |
MOD_Plk_1 | 310 | 316 | PF00069 | 0.267 |
MOD_Plk_1 | 318 | 324 | PF00069 | 0.249 |
MOD_Plk_1 | 328 | 334 | PF00069 | 0.215 |
MOD_Plk_1 | 374 | 380 | PF00069 | 0.390 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.451 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.390 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.379 |
MOD_Plk_4 | 310 | 316 | PF00069 | 0.279 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.325 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.260 |
MOD_Plk_4 | 502 | 508 | PF00069 | 0.321 |
MOD_Plk_4 | 532 | 538 | PF00069 | 0.301 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.390 |
MOD_ProDKin_1 | 479 | 485 | PF00069 | 0.390 |
MOD_ProDKin_1 | 537 | 543 | PF00069 | 0.294 |
MOD_SUMO_for_1 | 4 | 7 | PF00179 | 0.391 |
MOD_SUMO_rev_2 | 58 | 67 | PF00179 | 0.436 |
MOD_SUMO_rev_2 | 72 | 78 | PF00179 | 0.418 |
TRG_ENDOCYTIC_2 | 364 | 367 | PF00928 | 0.167 |
TRG_ENDOCYTIC_2 | 519 | 522 | PF00928 | 0.355 |
TRG_ER_diArg_1 | 133 | 135 | PF00400 | 0.333 |
TRG_ER_diArg_1 | 270 | 273 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 40 | 42 | PF00400 | 0.399 |
TRG_ER_diArg_1 | 411 | 414 | PF00400 | 0.245 |
TRG_ER_diArg_1 | 442 | 445 | PF00400 | 0.167 |
TRG_NES_CRM1_1 | 172 | 185 | PF08389 | 0.215 |
TRG_Pf-PMV_PEXEL_1 | 149 | 153 | PF00026 | 0.513 |
TRG_Pf-PMV_PEXEL_1 | 42 | 47 | PF00026 | 0.532 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4D7 | Leptomonas seymouri | 69% | 100% |
A0A0S4IQS3 | Bodo saltans | 38% | 100% |
A0A1X0P6P7 | Trypanosomatidae | 45% | 100% |
A0A3R7LHF8 | Trypanosoma rangeli | 44% | 100% |
A0A3S7X944 | Leishmania donovani | 86% | 100% |
A4IB79 | Leishmania infantum | 86% | 100% |
A7YWS7 | Bos taurus | 24% | 100% |
C9ZZK4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9AF00 | Leishmania major | 86% | 100% |
E9B656 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
O54956 | Mus musculus | 24% | 100% |
O94263 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 93% |
P0CN24 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 24% | 100% |
P0CN25 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 24% | 100% |
P24482 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 80% |
P56282 | Homo sapiens | 24% | 100% |
Q19196 | Caenorhabditis elegans | 22% | 100% |
Q500V9 | Arabidopsis thaliana | 26% | 100% |
Q54Y85 | Dictyostelium discoideum | 24% | 82% |
Q5ZKQ6 | Gallus gallus | 23% | 100% |
Q6BQR8 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 21% | 83% |
Q6CPH8 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 24% | 78% |
Q6FSK8 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 26% | 77% |
Q758V1 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 25% | 82% |
Q9VRQ7 | Drosophila melanogaster | 24% | 100% |
V5BHX7 | Trypanosoma cruzi | 44% | 100% |