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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 17 |
NetGPI | no | yes: 0, no: 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: Q4QBQ3
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 18 |
GO:0003824 | catalytic activity | 1 | 18 |
GO:0005488 | binding | 1 | 18 |
GO:0005524 | ATP binding | 5 | 18 |
GO:0016462 | pyrophosphatase activity | 5 | 18 |
GO:0016787 | hydrolase activity | 2 | 18 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 18 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 18 |
GO:0016887 | ATP hydrolysis activity | 7 | 18 |
GO:0017076 | purine nucleotide binding | 4 | 18 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 18 |
GO:0030554 | adenyl nucleotide binding | 5 | 18 |
GO:0032553 | ribonucleotide binding | 3 | 18 |
GO:0032555 | purine ribonucleotide binding | 4 | 18 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 18 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 18 |
GO:0036094 | small molecule binding | 2 | 18 |
GO:0043167 | ion binding | 2 | 18 |
GO:0043168 | anion binding | 3 | 18 |
GO:0097159 | organic cyclic compound binding | 2 | 18 |
GO:0097367 | carbohydrate derivative binding | 2 | 18 |
GO:1901265 | nucleoside phosphate binding | 3 | 18 |
GO:1901363 | heterocyclic compound binding | 2 | 18 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 182 | 186 | PF00656 | 0.749 |
CLV_C14_Caspase3-7 | 392 | 396 | PF00656 | 0.495 |
CLV_C14_Caspase3-7 | 410 | 414 | PF00656 | 0.504 |
CLV_C14_Caspase3-7 | 484 | 488 | PF00656 | 0.775 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.357 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 503 | 505 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 610 | 612 | PF00675 | 0.586 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.340 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.332 |
CLV_PCSK_KEX2_1 | 503 | 505 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 610 | 612 | PF00082 | 0.586 |
CLV_PCSK_PC1ET2_1 | 229 | 231 | PF00082 | 0.344 |
CLV_PCSK_PC1ET2_1 | 26 | 28 | PF00082 | 0.601 |
CLV_PCSK_PC7_1 | 426 | 432 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.391 |
DEG_APCC_DBOX_1 | 583 | 591 | PF00400 | 0.571 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.448 |
DEG_SPOP_SBC_1 | 9 | 13 | PF00917 | 0.399 |
DOC_ANK_TNKS_1 | 328 | 335 | PF00023 | 0.597 |
DOC_CKS1_1 | 698 | 703 | PF01111 | 0.638 |
DOC_CYCLIN_yClb1_LxF_4 | 336 | 341 | PF00134 | 0.548 |
DOC_CYCLIN_yCln2_LP_2 | 74 | 80 | PF00134 | 0.308 |
DOC_MAPK_gen_1 | 199 | 207 | PF00069 | 0.594 |
DOC_MAPK_gen_1 | 235 | 243 | PF00069 | 0.627 |
DOC_MAPK_gen_1 | 300 | 310 | PF00069 | 0.584 |
DOC_MAPK_gen_1 | 399 | 408 | PF00069 | 0.543 |
DOC_MAPK_gen_1 | 577 | 587 | PF00069 | 0.583 |
DOC_MAPK_MEF2A_6 | 201 | 209 | PF00069 | 0.562 |
DOC_MAPK_MEF2A_6 | 364 | 371 | PF00069 | 0.504 |
DOC_MAPK_MEF2A_6 | 580 | 587 | PF00069 | 0.588 |
DOC_PIKK_1 | 120 | 128 | PF02985 | 0.554 |
DOC_PP1_RVXF_1 | 289 | 295 | PF00149 | 0.605 |
DOC_PP1_RVXF_1 | 336 | 342 | PF00149 | 0.536 |
DOC_SPAK_OSR1_1 | 329 | 333 | PF12202 | 0.606 |
DOC_SPAK_OSR1_1 | 580 | 584 | PF12202 | 0.631 |
DOC_SPAK_OSR1_1 | 696 | 700 | PF12202 | 0.563 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 483 | 487 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.404 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 697 | 702 | PF00397 | 0.558 |
LIG_14-3-3_CanoR_1 | 166 | 172 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 238 | 244 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 364 | 370 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 435 | 442 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 580 | 584 | PF00244 | 0.582 |
LIG_APCC_ABBA_1 | 116 | 121 | PF00400 | 0.578 |
LIG_APCC_ABBA_1 | 211 | 216 | PF00400 | 0.445 |
LIG_APCC_ABBA_1 | 263 | 268 | PF00400 | 0.603 |
LIG_APCC_ABBA_1 | 406 | 411 | PF00400 | 0.515 |
LIG_deltaCOP1_diTrp_1 | 62 | 71 | PF00928 | 0.476 |
LIG_eIF4E_1 | 105 | 111 | PF01652 | 0.512 |
LIG_EVH1_1 | 65 | 69 | PF00568 | 0.343 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.618 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.567 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.725 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.295 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.530 |
LIG_FHA_2 | 251 | 257 | PF00498 | 0.529 |
LIG_FHA_2 | 698 | 704 | PF00498 | 0.613 |
LIG_LIR_Apic_2 | 170 | 176 | PF02991 | 0.635 |
LIG_LIR_Apic_2 | 569 | 573 | PF02991 | 0.607 |
LIG_LIR_Apic_2 | 62 | 66 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 127 | 137 | PF02991 | 0.608 |
LIG_LIR_Gen_1 | 29 | 38 | PF02991 | 0.547 |
LIG_LIR_Gen_1 | 588 | 596 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 70 | 79 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 91 | 101 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 127 | 133 | PF02991 | 0.627 |
LIG_LIR_Nem_3 | 163 | 168 | PF02991 | 0.633 |
LIG_LIR_Nem_3 | 208 | 213 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 29 | 35 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 62 | 67 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 70 | 74 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 91 | 96 | PF02991 | 0.553 |
LIG_NRBOX | 542 | 548 | PF00104 | 0.571 |
LIG_PCNA_PIPBox_1 | 711 | 720 | PF02747 | 0.576 |
LIG_PCNA_TLS_4 | 204 | 211 | PF02747 | 0.484 |
LIG_PDZ_Class_2 | 726 | 731 | PF00595 | 0.591 |
LIG_Pex14_1 | 280 | 284 | PF04695 | 0.559 |
LIG_Pex14_2 | 305 | 309 | PF04695 | 0.540 |
LIG_Pex14_2 | 385 | 389 | PF04695 | 0.469 |
LIG_Pex14_2 | 67 | 71 | PF04695 | 0.457 |
LIG_Pex3_1 | 46 | 57 | PF04882 | 0.314 |
LIG_Rb_pABgroove_1 | 403 | 411 | PF01858 | 0.515 |
LIG_REV1ctd_RIR_1 | 382 | 391 | PF16727 | 0.488 |
LIG_RPA_C_Fungi | 420 | 432 | PF08784 | 0.345 |
LIG_SH2_CRK | 173 | 177 | PF00017 | 0.505 |
LIG_SH2_CRK | 344 | 348 | PF00017 | 0.332 |
LIG_SH2_CRK | 98 | 102 | PF00017 | 0.409 |
LIG_SH2_NCK_1 | 119 | 123 | PF00017 | 0.464 |
LIG_SH2_NCK_1 | 173 | 177 | PF00017 | 0.491 |
LIG_SH2_SRC | 119 | 122 | PF00017 | 0.560 |
LIG_SH2_SRC | 210 | 213 | PF00017 | 0.332 |
LIG_SH2_STAP1 | 105 | 109 | PF00017 | 0.585 |
LIG_SH2_STAP1 | 381 | 385 | PF00017 | 0.352 |
LIG_SH2_STAT3 | 695 | 698 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.566 |
LIG_SH3_1 | 63 | 69 | PF00018 | 0.446 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.411 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.372 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.471 |
LIG_SH3_3 | 551 | 557 | PF00018 | 0.442 |
LIG_SH3_3 | 63 | 69 | PF00018 | 0.573 |
LIG_SUMO_SIM_anti_2 | 316 | 321 | PF11976 | 0.436 |
LIG_SUMO_SIM_anti_2 | 70 | 76 | PF11976 | 0.346 |
LIG_SUMO_SIM_par_1 | 560 | 566 | PF11976 | 0.424 |
LIG_TYR_ITIM | 601 | 606 | PF00017 | 0.593 |
LIG_TYR_ITIM | 96 | 101 | PF00017 | 0.404 |
LIG_WRC_WIRS_1 | 168 | 173 | PF05994 | 0.386 |
MOD_CDC14_SPxK_1 | 175 | 178 | PF00782 | 0.472 |
MOD_CDK_SPxK_1 | 172 | 178 | PF00069 | 0.475 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.695 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.569 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.378 |
MOD_CK1_1 | 687 | 693 | PF00069 | 0.727 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.493 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.403 |
MOD_CK2_1 | 697 | 703 | PF00069 | 0.414 |
MOD_Cter_Amidation | 501 | 504 | PF01082 | 0.829 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.566 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.598 |
MOD_GlcNHglycan | 542 | 546 | PF01048 | 0.378 |
MOD_GlcNHglycan | 612 | 615 | PF01048 | 0.633 |
MOD_GlcNHglycan | 687 | 690 | PF01048 | 0.767 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.516 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.452 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.475 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.442 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.704 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.654 |
MOD_GSK3_1 | 680 | 687 | PF00069 | 0.698 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.546 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.752 |
MOD_LATS_1 | 608 | 614 | PF00433 | 0.590 |
MOD_N-GLC_1 | 1 | 6 | PF02516 | 0.672 |
MOD_N-GLC_1 | 239 | 244 | PF02516 | 0.329 |
MOD_N-GLC_1 | 246 | 251 | PF02516 | 0.344 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.708 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.756 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.648 |
MOD_NEK2_1 | 541 | 546 | PF00069 | 0.487 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.313 |
MOD_NEK2_2 | 304 | 309 | PF00069 | 0.449 |
MOD_NEK2_2 | 579 | 584 | PF00069 | 0.462 |
MOD_PIKK_1 | 716 | 722 | PF00454 | 0.435 |
MOD_PKA_1 | 610 | 616 | PF00069 | 0.614 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.505 |
MOD_PKA_2 | 434 | 440 | PF00069 | 0.399 |
MOD_PKA_2 | 579 | 585 | PF00069 | 0.481 |
MOD_PKA_2 | 610 | 616 | PF00069 | 0.711 |
MOD_PKA_2 | 725 | 731 | PF00069 | 0.530 |
MOD_Plk_1 | 223 | 229 | PF00069 | 0.438 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.292 |
MOD_Plk_1 | 313 | 319 | PF00069 | 0.525 |
MOD_Plk_2-3 | 121 | 127 | PF00069 | 0.403 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.412 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.696 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.426 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.408 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.376 |
MOD_Plk_4 | 591 | 597 | PF00069 | 0.510 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.566 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.560 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.518 |
MOD_ProDKin_1 | 697 | 703 | PF00069 | 0.430 |
MOD_SUMO_for_1 | 192 | 195 | PF00179 | 0.495 |
TRG_DiLeu_BaEn_1 | 591 | 596 | PF01217 | 0.531 |
TRG_DiLeu_BaEn_2 | 402 | 408 | PF01217 | 0.358 |
TRG_DiLeu_BaLyEn_6 | 148 | 153 | PF01217 | 0.375 |
TRG_DiLeu_BaLyEn_6 | 45 | 50 | PF01217 | 0.460 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.662 |
TRG_ENDOCYTIC_2 | 168 | 171 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 381 | 384 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 589 | 592 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 603 | 606 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 98 | 101 | PF00928 | 0.672 |
TRG_ER_diArg_1 | 199 | 202 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 259 | 261 | PF00400 | 0.433 |
TRG_ER_diArg_1 | 326 | 329 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 425 | 427 | PF00400 | 0.371 |
TRG_ER_diArg_1 | 583 | 586 | PF00400 | 0.457 |
TRG_NES_CRM1_1 | 591 | 605 | PF08389 | 0.444 |
TRG_Pf-PMV_PEXEL_1 | 108 | 113 | PF00026 | 0.363 |
TRG_Pf-PMV_PEXEL_1 | 145 | 149 | PF00026 | 0.440 |
TRG_Pf-PMV_PEXEL_1 | 653 | 657 | PF00026 | 0.483 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P906 | Leptomonas seymouri | 31% | 99% |
A0A1X0NTT2 | Trypanosomatidae | 35% | 100% |
A0A3Q8IC80 | Leishmania donovani | 91% | 99% |
A0A3Q8IC95 | Leishmania donovani | 75% | 100% |
A0A3Q8IHZ0 | Leishmania donovani | 29% | 100% |
A0A422NUH1 | Trypanosoma rangeli | 34% | 100% |
A4HCE5 | Leishmania braziliensis | 75% | 100% |
A4HZW7 | Leishmania infantum | 75% | 100% |
A4IDZ9 | Leishmania infantum | 29% | 100% |
C9ZSJ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AU21 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AVS5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
E9AVS6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q0H4 | Leishmania major | 28% | 100% |
Q4QBQ4 | Leishmania major | 80% | 100% |
V5DMJ8 | Trypanosoma cruzi | 33% | 100% |