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 | yes | yes: 4, no: 5 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: Q4QHK3
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 2 |
GO:0006793 | phosphorus metabolic process | 3 | 2 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009132 | nucleoside diphosphate metabolic process | 5 | 2 |
GO:0009134 | nucleoside diphosphate catabolic process | 6 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019439 | aromatic compound catabolic process | 4 | 2 |
GO:0019637 | organophosphate metabolic process | 3 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044270 | cellular nitrogen compound catabolic process | 4 | 2 |
GO:0044281 | small molecule metabolic process | 2 | 2 |
GO:0046434 | organophosphate catabolic process | 4 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0046700 | heterocycle catabolic process | 4 | 2 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901292 | nucleoside phosphate catabolic process | 5 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1901361 | organic cyclic compound catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004382 | GDP phosphatase activity | 7 | 5 |
GO:0005488 | binding | 1 | 9 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0016462 | pyrophosphatase activity | 5 | 5 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 5 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 5 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0017110 | nucleoside diphosphate phosphatase activity | 6 | 5 |
GO:0030554 | adenyl nucleotide binding | 5 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 9 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 251 | 255 | PF00656 | 0.232 |
CLV_C14_Caspase3-7 | 348 | 352 | PF00656 | 0.189 |
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.523 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 472 | 474 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 505 | 507 | PF00082 | 0.254 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.541 |
CLV_PCSK_PC1ET2_1 | 132 | 134 | PF00082 | 0.501 |
CLV_PCSK_PC1ET2_1 | 472 | 474 | PF00082 | 0.276 |
CLV_PCSK_PC1ET2_1 | 505 | 507 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.239 |
CLV_PCSK_SKI1_1 | 410 | 414 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 502 | 506 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 528 | 532 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.630 |
DEG_APCC_DBOX_1 | 132 | 140 | PF00400 | 0.431 |
DEG_APCC_DBOX_1 | 78 | 86 | PF00400 | 0.477 |
DEG_SPOP_SBC_1 | 433 | 437 | PF00917 | 0.276 |
DOC_CYCLIN_yCln2_LP_2 | 529 | 535 | PF00134 | 0.298 |
DOC_MAPK_DCC_7 | 526 | 535 | PF00069 | 0.298 |
DOC_MAPK_gen_1 | 526 | 535 | PF00069 | 0.320 |
DOC_MAPK_gen_1 | 585 | 592 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 76 | 85 | PF00069 | 0.627 |
DOC_PP4_MxPP_1 | 477 | 480 | PF00568 | 0.265 |
DOC_PP4_MxPP_1 | 548 | 551 | PF00568 | 0.276 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.189 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.291 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.320 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.368 |
DOC_USP7_MATH_1 | 572 | 576 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 581 | 585 | PF00917 | 0.327 |
DOC_USP7_UBL2_3 | 189 | 193 | PF12436 | 0.276 |
DOC_USP7_UBL2_3 | 419 | 423 | PF12436 | 0.404 |
DOC_USP7_UBL2_3 | 587 | 591 | PF12436 | 0.466 |
LIG_14-3-3_CanoR_1 | 125 | 130 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 154 | 162 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 315 | 321 | PF00244 | 0.189 |
LIG_14-3-3_CanoR_1 | 345 | 354 | PF00244 | 0.307 |
LIG_14-3-3_CanoR_1 | 383 | 389 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 92 | 100 | PF00244 | 0.569 |
LIG_AP2alpha_2 | 146 | 148 | PF02296 | 0.419 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.619 |
LIG_BRCT_BRCA1_1 | 111 | 115 | PF00533 | 0.479 |
LIG_BRCT_BRCA1_1 | 194 | 198 | PF00533 | 0.255 |
LIG_BRCT_BRCA1_1 | 562 | 566 | PF00533 | 0.320 |
LIG_deltaCOP1_diTrp_1 | 257 | 263 | PF00928 | 0.320 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.625 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.255 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.352 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.264 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.283 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.372 |
LIG_FHA_1 | 554 | 560 | PF00498 | 0.279 |
LIG_FHA_2 | 17 | 23 | PF00498 | 0.606 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.372 |
LIG_FHA_2 | 346 | 352 | PF00498 | 0.230 |
LIG_Integrin_RGD_1 | 466 | 468 | PF01839 | 0.189 |
LIG_LIR_Gen_1 | 191 | 200 | PF02991 | 0.293 |
LIG_LIR_Gen_1 | 257 | 266 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 563 | 572 | PF02991 | 0.255 |
LIG_LIR_Gen_1 | 626 | 635 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 145 | 151 | PF02991 | 0.675 |
LIG_LIR_Nem_3 | 191 | 197 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 257 | 263 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 399 | 403 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 486 | 491 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 563 | 569 | PF02991 | 0.255 |
LIG_LIR_Nem_3 | 628 | 634 | PF02991 | 0.289 |
LIG_Pex14_2 | 562 | 566 | PF04695 | 0.320 |
LIG_PTB_Apo_2 | 306 | 313 | PF02174 | 0.276 |
LIG_RPA_C_Fungi | 65 | 77 | PF08784 | 0.397 |
LIG_SH2_CRK | 194 | 198 | PF00017 | 0.279 |
LIG_SH2_CRK | 632 | 636 | PF00017 | 0.381 |
LIG_SH2_NCK_1 | 194 | 198 | PF00017 | 0.279 |
LIG_SH2_NCK_1 | 643 | 647 | PF00017 | 0.309 |
LIG_SH2_SRC | 396 | 399 | PF00017 | 0.255 |
LIG_SH2_SRC | 495 | 498 | PF00017 | 0.351 |
LIG_SH2_SRC | 634 | 637 | PF00017 | 0.351 |
LIG_SH2_STAP1 | 194 | 198 | PF00017 | 0.276 |
LIG_SH2_STAP1 | 384 | 388 | PF00017 | 0.276 |
LIG_SH2_STAP1 | 560 | 564 | PF00017 | 0.277 |
LIG_SH2_STAP1 | 627 | 631 | PF00017 | 0.367 |
LIG_SH2_STAP1 | 632 | 636 | PF00017 | 0.344 |
LIG_SH2_STAP1 | 660 | 664 | PF00017 | 0.295 |
LIG_SH2_STAT3 | 414 | 417 | PF00017 | 0.189 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 634 | 637 | PF00017 | 0.309 |
LIG_SH3_1 | 472 | 478 | PF00018 | 0.275 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.279 |
LIG_SH3_3 | 472 | 478 | PF00018 | 0.378 |
LIG_SH3_3 | 509 | 515 | PF00018 | 0.359 |
LIG_SH3_3 | 544 | 550 | PF00018 | 0.256 |
LIG_SH3_3 | 587 | 593 | PF00018 | 0.309 |
LIG_SUMO_SIM_anti_2 | 109 | 115 | PF11976 | 0.471 |
LIG_SUMO_SIM_anti_2 | 229 | 236 | PF11976 | 0.298 |
LIG_SUMO_SIM_anti_2 | 350 | 358 | PF11976 | 0.369 |
LIG_SUMO_SIM_anti_2 | 567 | 572 | PF11976 | 0.210 |
LIG_SUMO_SIM_par_1 | 350 | 358 | PF11976 | 0.354 |
LIG_SUMO_SIM_par_1 | 669 | 674 | PF11976 | 0.338 |
LIG_SUMO_SIM_par_1 | 84 | 89 | PF11976 | 0.607 |
LIG_TRAF2_1 | 325 | 328 | PF00917 | 0.320 |
LIG_TYR_ITIM | 192 | 197 | PF00017 | 0.189 |
LIG_UBA3_1 | 166 | 175 | PF00899 | 0.551 |
LIG_UBA3_1 | 237 | 243 | PF00899 | 0.410 |
LIG_UBA3_1 | 290 | 295 | PF00899 | 0.441 |
LIG_UBA3_1 | 412 | 419 | PF00899 | 0.362 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.593 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.276 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.517 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.538 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.586 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.189 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.372 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.465 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.536 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.643 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.546 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.351 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.226 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.392 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.461 |
MOD_GSK3_1 | 662 | 669 | PF00069 | 0.303 |
MOD_N-GLC_1 | 120 | 125 | PF02516 | 0.584 |
MOD_N-GLC_1 | 308 | 313 | PF02516 | 0.254 |
MOD_N-GLC_1 | 316 | 321 | PF02516 | 0.206 |
MOD_N-GLC_1 | 553 | 558 | PF02516 | 0.388 |
MOD_N-GLC_1 | 572 | 577 | PF02516 | 0.320 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.531 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.167 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.255 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.508 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.261 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.347 |
MOD_NEK2_1 | 606 | 611 | PF00069 | 0.309 |
MOD_NEK2_1 | 630 | 635 | PF00069 | 0.251 |
MOD_NEK2_1 | 666 | 671 | PF00069 | 0.261 |
MOD_NEK2_2 | 188 | 193 | PF00069 | 0.189 |
MOD_NEK2_2 | 316 | 321 | PF00069 | 0.189 |
MOD_NEK2_2 | 371 | 376 | PF00069 | 0.232 |
MOD_NEK2_2 | 389 | 394 | PF00069 | 0.254 |
MOD_NEK2_2 | 619 | 624 | PF00069 | 0.384 |
MOD_PIKK_1 | 36 | 42 | PF00454 | 0.634 |
MOD_PIKK_1 | 361 | 367 | PF00454 | 0.255 |
MOD_PIKK_1 | 417 | 423 | PF00454 | 0.340 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.489 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.438 |
MOD_PKB_1 | 306 | 314 | PF00069 | 0.298 |
MOD_PKB_1 | 90 | 98 | PF00069 | 0.517 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.656 |
MOD_Plk_1 | 248 | 254 | PF00069 | 0.167 |
MOD_Plk_1 | 308 | 314 | PF00069 | 0.254 |
MOD_Plk_1 | 316 | 322 | PF00069 | 0.206 |
MOD_Plk_1 | 350 | 356 | PF00069 | 0.268 |
MOD_Plk_1 | 371 | 377 | PF00069 | 0.232 |
MOD_Plk_1 | 572 | 578 | PF00069 | 0.320 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.473 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.468 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.268 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.298 |
MOD_Plk_4 | 572 | 578 | PF00069 | 0.422 |
MOD_Plk_4 | 630 | 636 | PF00069 | 0.257 |
MOD_Plk_4 | 666 | 672 | PF00069 | 0.274 |
MOD_SUMO_for_1 | 623 | 626 | PF00179 | 0.367 |
MOD_SUMO_rev_2 | 584 | 593 | PF00179 | 0.309 |
TRG_DiLeu_BaEn_3 | 80 | 86 | PF01217 | 0.479 |
TRG_DiLeu_BaEn_4 | 235 | 241 | PF01217 | 0.276 |
TRG_DiLeu_BaLyEn_6 | 525 | 530 | PF01217 | 0.320 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.279 |
TRG_ENDOCYTIC_2 | 627 | 630 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 632 | 635 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 636 | 639 | PF00928 | 0.367 |
TRG_ER_diArg_1 | 303 | 306 | PF00400 | 0.315 |
TRG_ER_diArg_1 | 75 | 77 | PF00400 | 0.615 |
TRG_NES_CRM1_1 | 105 | 119 | PF08389 | 0.469 |
TRG_NLS_MonoExtC_3 | 131 | 137 | PF00514 | 0.346 |
TRG_NLS_MonoExtN_4 | 131 | 136 | PF00514 | 0.345 |
TRG_Pf-PMV_PEXEL_1 | 243 | 247 | PF00026 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 289 | 294 | PF00026 | 0.372 |
TRG_Pf-PMV_PEXEL_1 | 456 | 461 | PF00026 | 0.189 |
TRG_Pf-PMV_PEXEL_1 | 97 | 101 | PF00026 | 0.613 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0E8 | Leptomonas seymouri | 46% | 99% |
A0A0S4IR76 | Bodo saltans | 30% | 100% |
A0A1X0NQR7 | Trypanosomatidae | 33% | 100% |
A0A3R7NV38 | Trypanosoma rangeli | 33% | 100% |
A0A3S7WR18 | Leishmania donovani | 90% | 100% |
A4H5Z8 | Leishmania braziliensis | 69% | 98% |
A4HUC4 | Leishmania infantum | 90% | 100% |
C9ZVG6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9AN23 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
P32621 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 100% |
P40009 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 100% |
P55772 | Mus musculus | 25% | 100% |
Q28CF8 | Xenopus tropicalis | 21% | 100% |
Q5MY95 | Homo sapiens | 23% | 100% |
Q8TGH6 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 29% | 100% |
Q9HEM6 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 31% | 100% |
Q9Y227 | Homo sapiens | 21% | 100% |