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 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: E9AN23
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009132 | nucleoside diphosphate metabolic process | 5 | 1 |
GO:0009134 | nucleoside diphosphate catabolic process | 6 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019439 | aromatic compound catabolic process | 4 | 1 |
GO:0019637 | organophosphate metabolic process | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044270 | cellular nitrogen compound catabolic process | 4 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0046434 | organophosphate catabolic process | 4 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0046700 | heterocycle catabolic process | 4 | 1 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901292 | nucleoside phosphate catabolic process | 5 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901361 | organic cyclic compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0005488 | binding | 1 | 9 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
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 |
GO:0004382 | GDP phosphatase activity | 7 | 4 |
GO:0016462 | pyrophosphatase activity | 5 | 4 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 4 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 4 |
GO:0017110 | nucleoside diphosphate phosphatase activity | 6 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 242 | 246 | PF00656 | 0.256 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.545 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 468 | 470 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 507 | 509 | PF00082 | 0.265 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.559 |
CLV_PCSK_PC1ET2_1 | 132 | 134 | PF00082 | 0.543 |
CLV_PCSK_PC1ET2_1 | 468 | 470 | PF00082 | 0.289 |
CLV_PCSK_PC1ET2_1 | 507 | 509 | PF00082 | 0.265 |
CLV_PCSK_PC1ET2_1 | 76 | 78 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 530 | 534 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.651 |
DEG_APCC_DBOX_1 | 132 | 140 | PF00400 | 0.482 |
DEG_APCC_DBOX_1 | 78 | 86 | PF00400 | 0.496 |
DEG_SPOP_SBC_1 | 429 | 433 | PF00917 | 0.289 |
DOC_MAPK_gen_1 | 528 | 537 | PF00069 | 0.338 |
DOC_MAPK_gen_1 | 587 | 594 | PF00069 | 0.447 |
DOC_MAPK_gen_1 | 76 | 85 | PF00069 | 0.636 |
DOC_PP1_RVXF_1 | 404 | 411 | PF00149 | 0.277 |
DOC_PP2B_LxvP_1 | 477 | 480 | PF13499 | 0.156 |
DOC_PP4_MxPP_1 | 473 | 476 | PF00568 | 0.277 |
DOC_PP4_MxPP_1 | 550 | 553 | PF00568 | 0.289 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.310 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.338 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.287 |
DOC_USP7_MATH_1 | 574 | 578 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 583 | 587 | PF00917 | 0.334 |
DOC_USP7_UBL2_3 | 185 | 189 | PF12436 | 0.289 |
DOC_USP7_UBL2_3 | 415 | 419 | PF12436 | 0.363 |
DOC_USP7_UBL2_3 | 589 | 593 | PF12436 | 0.460 |
LIG_14-3-3_CanoR_1 | 125 | 130 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 154 | 162 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 373 | 380 | PF00244 | 0.323 |
LIG_14-3-3_CanoR_1 | 530 | 536 | PF00244 | 0.156 |
LIG_14-3-3_CanoR_1 | 92 | 100 | PF00244 | 0.589 |
LIG_BIR_III_4 | 455 | 459 | PF00653 | 0.156 |
LIG_BRCT_BRCA1_1 | 111 | 115 | PF00533 | 0.489 |
LIG_BRCT_BRCA1_1 | 190 | 194 | PF00533 | 0.262 |
LIG_BRCT_BRCA1_1 | 564 | 568 | PF00533 | 0.338 |
LIG_deltaCOP1_diTrp_1 | 253 | 259 | PF00928 | 0.338 |
LIG_EVH1_1 | 474 | 478 | PF00568 | 0.156 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.669 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.262 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.262 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.270 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.283 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.391 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.156 |
LIG_FHA_1 | 556 | 562 | PF00498 | 0.286 |
LIG_FHA_2 | 132 | 138 | PF00498 | 0.350 |
LIG_FHA_2 | 17 | 23 | PF00498 | 0.584 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.378 |
LIG_FHA_2 | 615 | 621 | PF00498 | 0.164 |
LIG_LIR_Gen_1 | 187 | 196 | PF02991 | 0.321 |
LIG_LIR_Gen_1 | 253 | 262 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 368 | 378 | PF02991 | 0.183 |
LIG_LIR_Gen_1 | 565 | 574 | PF02991 | 0.262 |
LIG_LIR_Gen_1 | 628 | 637 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 145 | 151 | PF02991 | 0.670 |
LIG_LIR_Nem_3 | 187 | 193 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 231 | 236 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 253 | 259 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 395 | 399 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 488 | 493 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 565 | 571 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 630 | 636 | PF02991 | 0.296 |
LIG_MYND_1 | 472 | 476 | PF01753 | 0.156 |
LIG_PDZ_Class_1 | 671 | 676 | PF00595 | 0.234 |
LIG_Pex14_2 | 564 | 568 | PF04695 | 0.461 |
LIG_PTB_Apo_2 | 302 | 309 | PF02174 | 0.289 |
LIG_SH2_CRK | 190 | 194 | PF00017 | 0.286 |
LIG_SH2_CRK | 634 | 638 | PF00017 | 0.387 |
LIG_SH2_NCK_1 | 190 | 194 | PF00017 | 0.286 |
LIG_SH2_NCK_1 | 645 | 649 | PF00017 | 0.325 |
LIG_SH2_SRC | 392 | 395 | PF00017 | 0.262 |
LIG_SH2_SRC | 497 | 500 | PF00017 | 0.357 |
LIG_SH2_SRC | 636 | 639 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 190 | 194 | PF00017 | 0.286 |
LIG_SH2_STAP1 | 380 | 384 | PF00017 | 0.289 |
LIG_SH2_STAP1 | 562 | 566 | PF00017 | 0.283 |
LIG_SH2_STAP1 | 629 | 633 | PF00017 | 0.373 |
LIG_SH2_STAP1 | 634 | 638 | PF00017 | 0.364 |
LIG_SH2_STAP1 | 662 | 666 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 636 | 639 | PF00017 | 0.316 |
LIG_SH3_1 | 469 | 475 | PF00018 | 0.283 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.286 |
LIG_SH3_3 | 469 | 475 | PF00018 | 0.376 |
LIG_SH3_3 | 476 | 482 | PF00018 | 0.258 |
LIG_SH3_3 | 508 | 514 | PF00018 | 0.369 |
LIG_SH3_3 | 546 | 552 | PF00018 | 0.263 |
LIG_SH3_3 | 589 | 595 | PF00018 | 0.325 |
LIG_SUMO_SIM_anti_2 | 110 | 115 | PF11976 | 0.480 |
LIG_SUMO_SIM_anti_2 | 348 | 354 | PF11976 | 0.358 |
LIG_SUMO_SIM_anti_2 | 569 | 574 | PF11976 | 0.229 |
LIG_SUMO_SIM_anti_2 | 80 | 87 | PF11976 | 0.426 |
LIG_SUMO_SIM_par_1 | 348 | 354 | PF11976 | 0.354 |
LIG_SUMO_SIM_par_1 | 84 | 89 | PF11976 | 0.619 |
LIG_TRAF2_1 | 128 | 131 | PF00917 | 0.520 |
LIG_TRAF2_1 | 321 | 324 | PF00917 | 0.338 |
LIG_UBA3_1 | 166 | 175 | PF00899 | 0.603 |
LIG_UBA3_1 | 286 | 291 | PF00899 | 0.338 |
LIG_UBA3_1 | 567 | 576 | PF00899 | 0.259 |
LIG_WW_2 | 475 | 478 | PF00397 | 0.211 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.360 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.289 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.433 |
MOD_CK1_1 | 606 | 612 | PF00069 | 0.184 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.565 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.680 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.429 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.378 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.399 |
MOD_CK2_1 | 614 | 620 | PF00069 | 0.204 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.300 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.385 |
MOD_GlcNHglycan | 457 | 461 | PF01048 | 0.343 |
MOD_GlcNHglycan | 605 | 608 | PF01048 | 0.211 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.551 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.659 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.604 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.368 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.395 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.470 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.156 |
MOD_GSK3_1 | 664 | 671 | PF00069 | 0.330 |
MOD_N-GLC_1 | 120 | 125 | PF02516 | 0.628 |
MOD_N-GLC_1 | 555 | 560 | PF02516 | 0.393 |
MOD_N-GLC_1 | 574 | 579 | PF02516 | 0.143 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.569 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.619 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.277 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.266 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.156 |
MOD_NEK2_1 | 608 | 613 | PF00069 | 0.325 |
MOD_NEK2_1 | 632 | 637 | PF00069 | 0.285 |
MOD_NEK2_1 | 668 | 673 | PF00069 | 0.284 |
MOD_NEK2_2 | 385 | 390 | PF00069 | 0.168 |
MOD_NEK2_2 | 621 | 626 | PF00069 | 0.389 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.262 |
MOD_PIKK_1 | 413 | 419 | PF00454 | 0.325 |
MOD_PK_1 | 109 | 115 | PF00069 | 0.395 |
MOD_PK_1 | 443 | 449 | PF00069 | 0.205 |
MOD_PKA_1 | 154 | 160 | PF00069 | 0.473 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.529 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.560 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.334 |
MOD_PKB_1 | 90 | 98 | PF00069 | 0.544 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.650 |
MOD_Plk_1 | 574 | 580 | PF00069 | 0.338 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.493 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.589 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.205 |
MOD_Plk_4 | 574 | 580 | PF00069 | 0.431 |
MOD_Plk_4 | 632 | 638 | PF00069 | 0.263 |
MOD_Plk_4 | 668 | 674 | PF00069 | 0.305 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.364 |
MOD_SUMO_for_1 | 44 | 47 | PF00179 | 0.555 |
MOD_SUMO_for_1 | 625 | 628 | PF00179 | 0.373 |
MOD_SUMO_rev_2 | 128 | 134 | PF00179 | 0.348 |
MOD_SUMO_rev_2 | 55 | 62 | PF00179 | 0.444 |
MOD_SUMO_rev_2 | 586 | 595 | PF00179 | 0.325 |
TRG_DiLeu_BaEn_3 | 80 | 86 | PF01217 | 0.498 |
TRG_DiLeu_BaEn_4 | 231 | 237 | PF01217 | 0.289 |
TRG_DiLeu_BaLyEn_6 | 527 | 532 | PF01217 | 0.338 |
TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.286 |
TRG_ENDOCYTIC_2 | 629 | 632 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 634 | 637 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 638 | 641 | PF00928 | 0.375 |
TRG_ER_diArg_1 | 153 | 155 | PF00400 | 0.682 |
TRG_NES_CRM1_1 | 105 | 119 | PF08389 | 0.488 |
TRG_Pf-PMV_PEXEL_1 | 127 | 131 | PF00026 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 285 | 290 | PF00026 | 0.378 |
TRG_Pf-PMV_PEXEL_1 | 97 | 101 | PF00026 | 0.635 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0E8 | Leptomonas seymouri | 47% | 99% |
A0A0S4IR76 | Bodo saltans | 30% | 100% |
A0A1X0NQR7 | Trypanosomatidae | 34% | 100% |
A0A3R7NV38 | Trypanosoma rangeli | 32% | 100% |
A0A3S7WR18 | Leishmania donovani | 86% | 100% |
A4H5Z8 | Leishmania braziliensis | 67% | 100% |
A4HUC4 | Leishmania infantum | 87% | 100% |
C9ZVG6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
P40009 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 100% |
Q4QHK3 | Leishmania major | 85% | 99% |
Q8TGG8 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 30% | 100% |
Q9HEM6 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 31% | 100% |