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:0032991 | protein-containing complex | 1 | 12 |
GO:0042575 | DNA polymerase complex | 3 | 12 |
GO:0043625 | delta 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: E9AXM0
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 | 11 |
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:0006271 | DNA strand elongation involved in DNA replication | 6 | 1 |
GO:0022616 | DNA strand elongation | 5 | 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:0003887 | DNA-directed DNA polymerase activity | 5 | 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:0034061 | DNA polymerase activity | 4 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 8 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 431 | 435 | PF00656 | 0.379 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 510 | 514 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 523 | 527 | PF00082 | 0.666 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.383 |
CLV_Separin_Metazoa | 110 | 114 | PF03568 | 0.339 |
DEG_APCC_DBOX_1 | 184 | 192 | PF00400 | 0.320 |
DEG_APCC_DBOX_1 | 24 | 32 | PF00400 | 0.417 |
DEG_APCC_DBOX_1 | 268 | 276 | PF00400 | 0.425 |
DEG_SPOP_SBC_1 | 577 | 581 | PF00917 | 0.226 |
DOC_CYCLIN_RxL_1 | 21 | 32 | PF00134 | 0.426 |
DOC_MAPK_FxFP_2 | 480 | 483 | PF00069 | 0.320 |
DOC_MAPK_gen_1 | 267 | 274 | PF00069 | 0.339 |
DOC_MAPK_gen_1 | 291 | 300 | PF00069 | 0.425 |
DOC_MAPK_gen_1 | 312 | 319 | PF00069 | 0.304 |
DOC_MAPK_gen_1 | 352 | 361 | PF00069 | 0.451 |
DOC_MAPK_gen_1 | 385 | 394 | PF00069 | 0.316 |
DOC_MAPK_gen_1 | 550 | 560 | PF00069 | 0.383 |
DOC_MAPK_HePTP_8 | 349 | 361 | PF00069 | 0.320 |
DOC_MAPK_MEF2A_6 | 195 | 204 | PF00069 | 0.425 |
DOC_MAPK_MEF2A_6 | 267 | 276 | PF00069 | 0.322 |
DOC_MAPK_MEF2A_6 | 352 | 361 | PF00069 | 0.320 |
DOC_MAPK_MEF2A_6 | 568 | 577 | PF00069 | 0.418 |
DOC_MAPK_NFAT4_5 | 269 | 277 | PF00069 | 0.361 |
DOC_PP2B_LxvP_1 | 381 | 384 | PF13499 | 0.329 |
DOC_PP4_FxxP_1 | 480 | 483 | PF00568 | 0.320 |
DOC_PP4_FxxP_1 | 525 | 528 | PF00568 | 0.617 |
DOC_PP4_FxxP_1 | 589 | 592 | PF00568 | 0.573 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.394 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.425 |
DOC_USP7_UBL2_3 | 312 | 316 | PF12436 | 0.310 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 492 | 497 | PF00397 | 0.389 |
LIG_14-3-3_CanoR_1 | 267 | 273 | PF00244 | 0.341 |
LIG_14-3-3_CanoR_1 | 352 | 358 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 510 | 515 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 523 | 528 | PF00244 | 0.675 |
LIG_AP2alpha_2 | 488 | 490 | PF02296 | 0.304 |
LIG_BRCT_BRCA1_1 | 29 | 33 | PF00533 | 0.530 |
LIG_BRCT_BRCA1_1 | 368 | 372 | PF00533 | 0.339 |
LIG_BRCT_BRCA1_1 | 395 | 399 | PF00533 | 0.435 |
LIG_BRCT_BRCA1_1 | 480 | 484 | PF00533 | 0.309 |
LIG_BRCT_BRCA1_1 | 539 | 543 | PF00533 | 0.449 |
LIG_BRCT_BRCA1_2 | 539 | 545 | PF00533 | 0.448 |
LIG_Clathr_ClatBox_1 | 111 | 115 | PF01394 | 0.304 |
LIG_Clathr_ClatBox_1 | 572 | 576 | PF01394 | 0.369 |
LIG_EH_1 | 396 | 400 | PF12763 | 0.425 |
LIG_EH1_1 | 53 | 61 | PF00400 | 0.276 |
LIG_eIF4E_1 | 94 | 100 | PF01652 | 0.339 |
LIG_FAT_LD_1 | 272 | 280 | PF03623 | 0.160 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.246 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.304 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.317 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.339 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.425 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.415 |
LIG_FHA_1 | 582 | 588 | PF00498 | 0.463 |
LIG_FHA_2 | 346 | 352 | PF00498 | 0.433 |
LIG_FHA_2 | 455 | 461 | PF00498 | 0.330 |
LIG_FHA_2 | 511 | 517 | PF00498 | 0.466 |
LIG_LIR_Apic_2 | 478 | 483 | PF02991 | 0.320 |
LIG_LIR_Apic_2 | 524 | 528 | PF02991 | 0.609 |
LIG_LIR_Apic_2 | 588 | 592 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 224 | 235 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 239 | 249 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 508 | 517 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 224 | 230 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 239 | 245 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 508 | 514 | PF02991 | 0.388 |
LIG_MYND_1 | 380 | 384 | PF01753 | 0.320 |
LIG_NRBOX | 345 | 351 | PF00104 | 0.425 |
LIG_PCNA_yPIPBox_3 | 121 | 135 | PF02747 | 0.160 |
LIG_Pex14_2 | 480 | 484 | PF04695 | 0.320 |
LIG_PTAP_UEV_1 | 472 | 477 | PF05743 | 0.304 |
LIG_SH2_CRK | 205 | 209 | PF00017 | 0.425 |
LIG_SH2_STAP1 | 49 | 53 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.416 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.448 |
LIG_SH3_3 | 371 | 377 | PF00018 | 0.295 |
LIG_SH3_3 | 392 | 398 | PF00018 | 0.304 |
LIG_SH3_3 | 470 | 476 | PF00018 | 0.304 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.441 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.387 |
LIG_SUMO_SIM_anti_2 | 271 | 277 | PF11976 | 0.342 |
LIG_SUMO_SIM_anti_2 | 358 | 363 | PF11976 | 0.320 |
LIG_SUMO_SIM_par_1 | 355 | 360 | PF11976 | 0.335 |
LIG_SUMO_SIM_par_1 | 463 | 468 | PF11976 | 0.451 |
LIG_SUMO_SIM_par_1 | 571 | 576 | PF11976 | 0.383 |
LIG_TRAF2_1 | 513 | 516 | PF00917 | 0.572 |
LIG_WRC_WIRS_1 | 563 | 568 | PF05994 | 0.377 |
LIG_WRC_WIRS_1 | 586 | 591 | PF05994 | 0.500 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.663 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.454 |
MOD_CK1_1 | 532 | 538 | PF00069 | 0.730 |
MOD_CK1_1 | 585 | 591 | PF00069 | 0.511 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.361 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.538 |
MOD_CK2_1 | 345 | 351 | PF00069 | 0.439 |
MOD_CK2_1 | 510 | 516 | PF00069 | 0.467 |
MOD_CK2_1 | 577 | 583 | PF00069 | 0.227 |
MOD_GlcNHglycan | 122 | 127 | PF01048 | 0.397 |
MOD_GlcNHglycan | 134 | 138 | PF01048 | 0.236 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.514 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.346 |
MOD_GlcNHglycan | 180 | 185 | PF01048 | 0.271 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.509 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.373 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.503 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.327 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.343 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.361 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.380 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.720 |
MOD_GlcNHglycan | 568 | 571 | PF01048 | 0.450 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.648 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.339 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.353 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.499 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.395 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.345 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.366 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.335 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.304 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.423 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.502 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.377 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.405 |
MOD_N-GLC_1 | 284 | 289 | PF02516 | 0.413 |
MOD_N-GLC_1 | 3 | 8 | PF02516 | 0.549 |
MOD_N-GLC_1 | 577 | 582 | PF02516 | 0.334 |
MOD_N-GLC_2 | 211 | 213 | PF02516 | 0.178 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.376 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.432 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.533 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.454 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.413 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.306 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.354 |
MOD_NEK2_1 | 582 | 587 | PF00069 | 0.373 |
MOD_NEK2_2 | 284 | 289 | PF00069 | 0.421 |
MOD_NEK2_2 | 529 | 534 | PF00069 | 0.489 |
MOD_PIKK_1 | 31 | 37 | PF00454 | 0.418 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.644 |
MOD_PKA_2 | 268 | 274 | PF00069 | 0.385 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.304 |
MOD_Plk_1 | 284 | 290 | PF00069 | 0.413 |
MOD_Plk_1 | 577 | 583 | PF00069 | 0.459 |
MOD_Plk_2-3 | 414 | 420 | PF00069 | 0.276 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.389 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.421 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.382 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.449 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.473 |
MOD_ProDKin_1 | 492 | 498 | PF00069 | 0.389 |
MOD_SUMO_for_1 | 544 | 547 | PF00179 | 0.436 |
MOD_SUMO_rev_2 | 304 | 313 | PF00179 | 0.389 |
MOD_SUMO_rev_2 | 323 | 332 | PF00179 | 0.239 |
MOD_SUMO_rev_2 | 546 | 552 | PF00179 | 0.649 |
TRG_DiLeu_BaLyEn_6 | 230 | 235 | PF01217 | 0.478 |
TRG_DiLeu_BaLyEn_6 | 377 | 382 | PF01217 | 0.339 |
TRG_DiLeu_BaLyEn_6 | 556 | 561 | PF01217 | 0.395 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 37 | 40 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 511 | 514 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 94 | 97 | PF00928 | 0.327 |
TRG_ER_diArg_1 | 41 | 44 | PF00400 | 0.379 |
TRG_NES_CRM1_1 | 347 | 360 | PF08389 | 0.425 |
TRG_NLS_MonoExtC_3 | 313 | 318 | PF00514 | 0.320 |
TRG_NLS_MonoExtC_3 | 425 | 431 | PF00514 | 0.427 |
TRG_NLS_MonoExtN_4 | 312 | 319 | PF00514 | 0.320 |
TRG_Pf-PMV_PEXEL_1 | 102 | 106 | PF00026 | 0.320 |
TRG_Pf-PMV_PEXEL_1 | 185 | 189 | PF00026 | 0.339 |
TRG_Pf-PMV_PEXEL_1 | 77 | 82 | PF00026 | 0.425 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P663 | Leptomonas seymouri | 70% | 100% |
A0A0S4IRV7 | Bodo saltans | 38% | 100% |
A0A1X0NMG0 | Trypanosomatidae | 47% | 100% |
A0A3Q8ING8 | Leishmania donovani | 92% | 100% |
A0A422P247 | Trypanosoma rangeli | 47% | 100% |
A4HEE9 | Leishmania braziliensis | 86% | 100% |
A4I1I5 | Leishmania infantum | 93% | 100% |
C9ZJY3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
O35654 | Mus musculus | 27% | 100% |
O48520 | Arabidopsis thaliana | 25% | 100% |
O93610 | Xenopus laevis | 26% | 100% |
P46957 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 100% |
P87324 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 100% |
Q4Q9V2 | Leishmania major | 92% | 100% |
Q6AXY4 | Rattus norvegicus | 26% | 100% |
Q9LRE5 | Oryza sativa subsp. japonica | 27% | 100% |
Q9W088 | Drosophila melanogaster | 26% | 100% |
V5B3K0 | Trypanosoma cruzi | 46% | 100% |