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: 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: A4H5Z8
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: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 | 470 | 474 | PF00656 | 0.291 |
CLV_C14_Caspase3-7 | 500 | 504 | PF00656 | 0.266 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.697 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.690 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.457 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.703 |
CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.690 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 522 | 524 | PF00082 | 0.487 |
CLV_PCSK_PC1ET2_1 | 434 | 436 | PF00082 | 0.390 |
CLV_PCSK_PC1ET2_1 | 522 | 524 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.726 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.668 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 545 | 549 | PF00082 | 0.513 |
DOC_CYCLIN_yCln2_LP_2 | 546 | 552 | PF00134 | 0.343 |
DOC_MAPK_DCC_7 | 543 | 552 | PF00069 | 0.343 |
DOC_MAPK_gen_1 | 11 | 21 | PF00069 | 0.432 |
DOC_MAPK_gen_1 | 543 | 552 | PF00069 | 0.371 |
DOC_MAPK_MEF2A_6 | 14 | 23 | PF00069 | 0.505 |
DOC_MAPK_MEF2A_6 | 490 | 497 | PF00069 | 0.190 |
DOC_PP1_RVXF_1 | 423 | 430 | PF00149 | 0.301 |
DOC_PP4_FxxP_1 | 565 | 568 | PF00568 | 0.190 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.346 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.359 |
DOC_USP7_MATH_1 | 471 | 475 | PF00917 | 0.254 |
DOC_USP7_MATH_1 | 589 | 593 | PF00917 | 0.361 |
DOC_USP7_MATH_1 | 598 | 602 | PF00917 | 0.318 |
DOC_USP7_UBL2_3 | 604 | 608 | PF12436 | 0.376 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.269 |
DOC_WW_Pin1_4 | 456 | 461 | PF00397 | 0.304 |
LIG_14-3-3_CanoR_1 | 107 | 115 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 135 | 144 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 169 | 177 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 398 | 404 | PF00244 | 0.362 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.649 |
LIG_BIR_III_2 | 503 | 507 | PF00653 | 0.224 |
LIG_BRCT_BRCA1_1 | 209 | 213 | PF00533 | 0.270 |
LIG_BRCT_BRCA1_1 | 579 | 583 | PF00533 | 0.371 |
LIG_deltaCOP1_diTrp_1 | 272 | 278 | PF00928 | 0.371 |
LIG_eIF4E_1 | 577 | 583 | PF01652 | 0.190 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.529 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.270 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.270 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.331 |
LIG_FHA_1 | 366 | 372 | PF00498 | 0.276 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.269 |
LIG_FHA_1 | 422 | 428 | PF00498 | 0.329 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.364 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.269 |
LIG_FHA_1 | 571 | 577 | PF00498 | 0.287 |
LIG_FHA_1 | 650 | 656 | PF00498 | 0.270 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.443 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.341 |
LIG_FHA_2 | 451 | 457 | PF00498 | 0.355 |
LIG_FHA_2 | 551 | 557 | PF00498 | 0.190 |
LIG_GBD_Chelix_1 | 19 | 27 | PF00786 | 0.212 |
LIG_LIR_Gen_1 | 272 | 281 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 491 | 502 | PF02991 | 0.190 |
LIG_LIR_Gen_1 | 580 | 589 | PF02991 | 0.270 |
LIG_LIR_Gen_1 | 643 | 651 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 652 | 660 | PF02991 | 0.241 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 272 | 278 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 414 | 418 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 491 | 497 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 503 | 508 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 580 | 586 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 645 | 651 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 652 | 656 | PF02991 | 0.262 |
LIG_NRBOX | 581 | 587 | PF00104 | 0.190 |
LIG_Pex14_2 | 579 | 583 | PF04695 | 0.371 |
LIG_PTB_Apo_2 | 599 | 606 | PF02174 | 0.176 |
LIG_SH2_CRK | 209 | 213 | PF00017 | 0.287 |
LIG_SH2_CRK | 257 | 261 | PF00017 | 0.190 |
LIG_SH2_CRK | 653 | 657 | PF00017 | 0.327 |
LIG_SH2_NCK_1 | 209 | 213 | PF00017 | 0.287 |
LIG_SH2_NCK_1 | 660 | 664 | PF00017 | 0.357 |
LIG_SH2_SRC | 411 | 414 | PF00017 | 0.263 |
LIG_SH2_STAP1 | 209 | 213 | PF00017 | 0.285 |
LIG_SH2_STAP1 | 512 | 516 | PF00017 | 0.190 |
LIG_SH2_STAP1 | 577 | 581 | PF00017 | 0.286 |
LIG_SH2_STAP1 | 644 | 648 | PF00017 | 0.339 |
LIG_SH2_STAP1 | 649 | 653 | PF00017 | 0.331 |
LIG_SH2_STAP1 | 677 | 681 | PF00017 | 0.304 |
LIG_SH2_STAT3 | 512 | 515 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 651 | 654 | PF00017 | 0.307 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.387 |
LIG_SH3_3 | 379 | 385 | PF00018 | 0.287 |
LIG_SH3_3 | 561 | 567 | PF00018 | 0.271 |
LIG_SH3_3 | 604 | 610 | PF00018 | 0.357 |
LIG_SUMO_SIM_anti_2 | 244 | 251 | PF11976 | 0.343 |
LIG_SUMO_SIM_par_1 | 686 | 691 | PF11976 | 0.315 |
LIG_SUMO_SIM_par_1 | 98 | 104 | PF11976 | 0.516 |
LIG_TRAF2_1 | 340 | 343 | PF00917 | 0.371 |
LIG_TRAF2_1 | 553 | 556 | PF00917 | 0.355 |
LIG_TYR_ITIM | 255 | 260 | PF00017 | 0.318 |
LIG_UBA3_1 | 141 | 145 | PF00899 | 0.350 |
LIG_UBA3_1 | 252 | 258 | PF00899 | 0.358 |
LIG_UBA3_1 | 305 | 310 | PF00899 | 0.371 |
LIG_UBA3_1 | 427 | 434 | PF00899 | 0.334 |
LIG_WRC_WIRS_1 | 355 | 360 | PF05994 | 0.190 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.471 |
MOD_CK1_1 | 458 | 464 | PF00069 | 0.250 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.415 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.341 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.318 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.241 |
MOD_CK2_1 | 550 | 556 | PF00069 | 0.190 |
MOD_CK2_1 | 672 | 678 | PF00069 | 0.232 |
MOD_Cter_Amidation | 432 | 435 | PF01082 | 0.390 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.727 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.663 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.469 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.466 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.493 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.466 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.555 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.492 |
MOD_GlcNHglycan | 674 | 677 | PF01048 | 0.376 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.683 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.472 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.314 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.248 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.161 |
MOD_GSK3_1 | 672 | 679 | PF00069 | 0.312 |
MOD_N-GLC_1 | 135 | 140 | PF02516 | 0.717 |
MOD_N-GLC_1 | 467 | 472 | PF02516 | 0.522 |
MOD_N-GLC_1 | 570 | 575 | PF02516 | 0.548 |
MOD_N-GLC_1 | 589 | 594 | PF02516 | 0.346 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.369 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.270 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.308 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.266 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.224 |
MOD_NEK2_1 | 623 | 628 | PF00069 | 0.350 |
MOD_NEK2_1 | 647 | 652 | PF00069 | 0.266 |
MOD_NEK2_1 | 683 | 688 | PF00069 | 0.274 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.373 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.387 |
MOD_NEK2_2 | 386 | 391 | PF00069 | 0.260 |
MOD_NEK2_2 | 404 | 409 | PF00069 | 0.287 |
MOD_NEK2_2 | 636 | 641 | PF00069 | 0.346 |
MOD_PIKK_1 | 230 | 236 | PF00454 | 0.190 |
MOD_PIKK_1 | 376 | 382 | PF00454 | 0.270 |
MOD_PKA_1 | 169 | 175 | PF00069 | 0.461 |
MOD_PKA_1 | 323 | 329 | PF00069 | 0.190 |
MOD_PKA_1 | 672 | 678 | PF00069 | 0.176 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.351 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.477 |
MOD_PKA_2 | 329 | 335 | PF00069 | 0.266 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.273 |
MOD_PKA_2 | 397 | 403 | PF00069 | 0.301 |
MOD_PKA_2 | 445 | 451 | PF00069 | 0.190 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.465 |
MOD_PKA_2 | 518 | 524 | PF00069 | 0.190 |
MOD_PKB_1 | 105 | 113 | PF00069 | 0.527 |
MOD_PKB_1 | 321 | 329 | PF00069 | 0.343 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.339 |
MOD_Plk_1 | 589 | 595 | PF00069 | 0.371 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.280 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.338 |
MOD_Plk_4 | 386 | 392 | PF00069 | 0.190 |
MOD_Plk_4 | 683 | 689 | PF00069 | 0.268 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.269 |
MOD_ProDKin_1 | 456 | 462 | PF00069 | 0.304 |
MOD_SUMO_for_1 | 151 | 154 | PF00179 | 0.345 |
MOD_SUMO_for_1 | 59 | 62 | PF00179 | 0.443 |
MOD_SUMO_for_1 | 640 | 643 | PF00179 | 0.339 |
MOD_SUMO_rev_2 | 601 | 610 | PF00179 | 0.357 |
TRG_DiLeu_BaEn_3 | 477 | 483 | PF01217 | 0.190 |
TRG_DiLeu_BaLyEn_6 | 542 | 547 | PF01217 | 0.371 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.287 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.230 |
TRG_ENDOCYTIC_2 | 644 | 647 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 653 | 656 | PF00928 | 0.339 |
TRG_ER_diArg_1 | 168 | 170 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 318 | 321 | PF00400 | 0.311 |
TRG_Pf-PMV_PEXEL_1 | 112 | 116 | PF00026 | 0.719 |
TRG_Pf-PMV_PEXEL_1 | 258 | 262 | PF00026 | 0.543 |
TRG_Pf-PMV_PEXEL_1 | 304 | 309 | PF00026 | 0.541 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0E8 | Leptomonas seymouri | 46% | 100% |
A0A1X0NQR7 | Trypanosomatidae | 32% | 100% |
A0A3R7NV38 | Trypanosoma rangeli | 34% | 100% |
A0A3S7WR18 | Leishmania donovani | 70% | 100% |
A4HUC4 | Leishmania infantum | 70% | 100% |
C9ZVG6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9AN23 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 100% |
P40009 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 100% |
Q28CF8 | Xenopus tropicalis | 20% | 100% |
Q4QHK3 | Leishmania major | 69% | 99% |
Q5REF6 | Pongo abelii | 22% | 100% |
Q8TGH6 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 30% | 100% |
Q9DBT4 | Mus musculus | 21% | 100% |
Q9HEM6 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 30% | 100% |
Q9NQZ7 | Homo sapiens | 22% | 100% |
Q9Y227 | Homo sapiens | 22% | 100% |