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 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: E9AVS5
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 | 380 | 384 | PF00656 | 0.591 |
CLV_C14_Caspase3-7 | 398 | 402 | PF00656 | 0.411 |
CLV_C14_Caspase3-7 | 472 | 476 | PF00656 | 0.699 |
CLV_C14_Caspase3-7 | 6 | 10 | PF00656 | 0.364 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.398 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.295 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 605 | 607 | PF00675 | 0.590 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.311 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.315 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 605 | 607 | PF00082 | 0.590 |
CLV_PCSK_PC7_1 | 414 | 420 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 68 | 72 | PF00082 | 0.410 |
DEG_APCC_DBOX_1 | 186 | 194 | PF00400 | 0.516 |
DEG_APCC_DBOX_1 | 578 | 586 | PF00400 | 0.559 |
DOC_ANK_TNKS_1 | 316 | 323 | PF00023 | 0.580 |
DOC_CKS1_1 | 689 | 694 | PF01111 | 0.641 |
DOC_CYCLIN_RxL_1 | 65 | 73 | PF00134 | 0.656 |
DOC_CYCLIN_yClb1_LxF_4 | 324 | 329 | PF00134 | 0.527 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 535 | 542 | PF00134 | 0.520 |
DOC_CYCLIN_yCln2_LP_2 | 147 | 153 | PF00134 | 0.533 |
DOC_MAPK_gen_1 | 288 | 298 | PF00069 | 0.665 |
DOC_MAPK_gen_1 | 387 | 396 | PF00069 | 0.526 |
DOC_MAPK_gen_1 | 572 | 582 | PF00069 | 0.565 |
DOC_MAPK_MEF2A_6 | 352 | 359 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 575 | 582 | PF00069 | 0.575 |
DOC_PP1_RVXF_1 | 277 | 283 | PF00149 | 0.590 |
DOC_PP1_RVXF_1 | 324 | 330 | PF00149 | 0.525 |
DOC_SPAK_OSR1_1 | 317 | 321 | PF12202 | 0.588 |
DOC_SPAK_OSR1_1 | 575 | 579 | PF12202 | 0.611 |
DOC_SPAK_OSR1_1 | 687 | 691 | PF12202 | 0.579 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.497 |
DOC_USP7_UBL2_3 | 192 | 196 | PF12436 | 0.497 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 688 | 693 | PF00397 | 0.560 |
LIG_14-3-3_CanoR_1 | 226 | 232 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 352 | 358 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 423 | 430 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 575 | 579 | PF00244 | 0.557 |
LIG_14-3-3_CterR_2 | 717 | 722 | PF00244 | 0.499 |
LIG_Actin_RPEL_3 | 445 | 464 | PF02755 | 0.564 |
LIG_APCC_ABBA_1 | 251 | 256 | PF00400 | 0.590 |
LIG_APCC_ABBA_1 | 394 | 399 | PF00400 | 0.501 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.359 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.359 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.359 |
LIG_BRCT_BRCA1_1 | 134 | 138 | PF00533 | 0.504 |
LIG_EVH1_2 | 101 | 105 | PF00568 | 0.542 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.579 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.481 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.563 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.682 |
LIG_FHA_1 | 455 | 461 | PF00498 | 0.648 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.598 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.377 |
LIG_FHA_2 | 689 | 695 | PF00498 | 0.611 |
LIG_LIR_Apic_2 | 162 | 168 | PF02991 | 0.601 |
LIG_LIR_Apic_2 | 35 | 40 | PF02991 | 0.455 |
LIG_LIR_Apic_2 | 564 | 568 | PF02991 | 0.587 |
LIG_LIR_Gen_1 | 12 | 22 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 48 | 59 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 583 | 591 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 12 | 17 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 48 | 54 | PF02991 | 0.329 |
LIG_MLH1_MIPbox_1 | 134 | 138 | PF16413 | 0.504 |
LIG_NRBOX | 537 | 543 | PF00104 | 0.553 |
LIG_PCNA_PIPBox_1 | 702 | 711 | PF02747 | 0.571 |
LIG_PDZ_Class_2 | 717 | 722 | PF00595 | 0.588 |
LIG_Pex14_1 | 268 | 272 | PF04695 | 0.550 |
LIG_Pex14_2 | 293 | 297 | PF04695 | 0.526 |
LIG_Pex14_2 | 373 | 377 | PF04695 | 0.459 |
LIG_Rb_pABgroove_1 | 391 | 399 | PF01858 | 0.501 |
LIG_RPA_C_Fungi | 408 | 420 | PF08784 | 0.328 |
LIG_SH2_CRK | 332 | 336 | PF00017 | 0.308 |
LIG_SH2_CRK | 369 | 373 | PF00017 | 0.203 |
LIG_SH2_GRB2like | 139 | 142 | PF00017 | 0.495 |
LIG_SH2_NCK_1 | 369 | 373 | PF00017 | 0.203 |
LIG_SH2_PTP2 | 157 | 160 | PF00017 | 0.390 |
LIG_SH2_PTP2 | 165 | 168 | PF00017 | 0.399 |
LIG_SH2_PTP2 | 37 | 40 | PF00017 | 0.365 |
LIG_SH2_PTP2 | 51 | 54 | PF00017 | 0.339 |
LIG_SH2_SRC | 369 | 372 | PF00017 | 0.203 |
LIG_SH2_SRC | 37 | 40 | PF00017 | 0.359 |
LIG_SH2_STAP1 | 29 | 33 | PF00017 | 0.431 |
LIG_SH2_STAP1 | 369 | 373 | PF00017 | 0.333 |
LIG_SH2_STAT3 | 29 | 32 | PF00017 | 0.574 |
LIG_SH2_STAT3 | 686 | 689 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 37 | 40 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 51 | 54 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.471 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.465 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.351 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.472 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.353 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.458 |
LIG_SH3_3 | 546 | 552 | PF00018 | 0.432 |
LIG_SH3_3 | 63 | 69 | PF00018 | 0.437 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.325 |
LIG_SUMO_SIM_anti_2 | 304 | 309 | PF11976 | 0.414 |
LIG_SUMO_SIM_par_1 | 142 | 149 | PF11976 | 0.358 |
LIG_SUMO_SIM_par_1 | 555 | 561 | PF11976 | 0.400 |
LIG_TYR_ITIM | 596 | 601 | PF00017 | 0.607 |
LIG_UBA3_1 | 190 | 196 | PF00899 | 0.350 |
LIG_WRPW_2 | 151 | 154 | PF00400 | 0.328 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.618 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.521 |
MOD_CK1_1 | 678 | 684 | PF00069 | 0.624 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.542 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.409 |
MOD_CK2_1 | 688 | 694 | PF00069 | 0.414 |
MOD_Cter_Amidation | 489 | 492 | PF01082 | 0.815 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.513 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.360 |
MOD_GlcNHglycan | 678 | 681 | PF01048 | 0.721 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.517 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.542 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.490 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.611 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.664 |
MOD_GSK3_1 | 672 | 679 | PF00069 | 0.709 |
MOD_LATS_1 | 603 | 609 | PF00433 | 0.586 |
MOD_N-GLC_1 | 171 | 176 | PF02516 | 0.495 |
MOD_N-GLC_1 | 536 | 541 | PF02516 | 0.285 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.429 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.553 |
MOD_NEK2_1 | 536 | 541 | PF00069 | 0.476 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.514 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.453 |
MOD_NEK2_2 | 292 | 297 | PF00069 | 0.432 |
MOD_NEK2_2 | 574 | 579 | PF00069 | 0.424 |
MOD_PIKK_1 | 180 | 186 | PF00454 | 0.462 |
MOD_PIKK_1 | 707 | 713 | PF00454 | 0.430 |
MOD_PKA_1 | 605 | 611 | PF00069 | 0.603 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.446 |
MOD_PKA_2 | 422 | 428 | PF00069 | 0.369 |
MOD_PKA_2 | 574 | 580 | PF00069 | 0.444 |
MOD_PKA_2 | 605 | 611 | PF00069 | 0.712 |
MOD_PKA_2 | 716 | 722 | PF00069 | 0.521 |
MOD_Plk_1 | 211 | 217 | PF00069 | 0.416 |
MOD_Plk_1 | 301 | 307 | PF00069 | 0.476 |
MOD_Plk_1 | 454 | 460 | PF00069 | 0.524 |
MOD_Plk_2-3 | 376 | 382 | PF00069 | 0.287 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.415 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.405 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.517 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.641 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.481 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.565 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.480 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.311 |
MOD_ProDKin_1 | 688 | 694 | PF00069 | 0.430 |
MOD_SUMO_for_1 | 210 | 213 | PF00179 | 0.321 |
TRG_DiLeu_BaEn_1 | 186 | 191 | PF01217 | 0.368 |
TRG_DiLeu_BaEn_1 | 586 | 591 | PF01217 | 0.528 |
TRG_DiLeu_BaEn_2 | 390 | 396 | PF01217 | 0.333 |
TRG_DiLeu_BaLyEn_6 | 66 | 71 | PF01217 | 0.566 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 51 | 54 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.255 |
TRG_ENDOCYTIC_2 | 584 | 587 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 598 | 601 | PF00928 | 0.455 |
TRG_ER_diArg_1 | 187 | 190 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 231 | 234 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 314 | 317 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 413 | 415 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 578 | 581 | PF00400 | 0.434 |
TRG_NES_CRM1_1 | 586 | 600 | PF08389 | 0.432 |
TRG_Pf-PMV_PEXEL_1 | 646 | 650 | PF00026 | 0.484 |
TRG_Pf-PMV_PEXEL_1 | 68 | 72 | PF00026 | 0.473 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P906 | Leptomonas seymouri | 30% | 98% |
A0A1X0NTT2 | Trypanosomatidae | 35% | 100% |
A0A3Q8IC80 | Leishmania donovani | 71% | 98% |
A0A3Q8IC95 | Leishmania donovani | 86% | 100% |
A0A3Q8IHZ0 | Leishmania donovani | 29% | 100% |
A0A422NUH1 | Trypanosoma rangeli | 35% | 100% |
A4HCE5 | Leishmania braziliensis | 60% | 100% |
A4HZW7 | Leishmania infantum | 87% | 100% |
A4IDZ9 | Leishmania infantum | 29% | 100% |
C9ZSJ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AU21 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AVS6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 98% |
Q4Q0H4 | Leishmania major | 28% | 100% |
Q4QBQ3 | Leishmania major | 72% | 100% |
Q4QBQ4 | Leishmania major | 86% | 99% |
V5DMJ8 | Trypanosoma cruzi | 34% | 100% |