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: 18 |
NetGPI | no | yes: 0, no: 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: A4HCE5
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 19 |
GO:0003824 | catalytic activity | 1 | 19 |
GO:0005488 | binding | 1 | 19 |
GO:0005524 | ATP binding | 5 | 19 |
GO:0016462 | pyrophosphatase activity | 5 | 19 |
GO:0016787 | hydrolase activity | 2 | 19 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 19 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 19 |
GO:0016887 | ATP hydrolysis activity | 7 | 19 |
GO:0017076 | purine nucleotide binding | 4 | 19 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 19 |
GO:0030554 | adenyl nucleotide binding | 5 | 19 |
GO:0032553 | ribonucleotide binding | 3 | 19 |
GO:0032555 | purine ribonucleotide binding | 4 | 19 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 19 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 19 |
GO:0036094 | small molecule binding | 2 | 19 |
GO:0043167 | ion binding | 2 | 19 |
GO:0043168 | anion binding | 3 | 19 |
GO:0097159 | organic cyclic compound binding | 2 | 19 |
GO:0097367 | carbohydrate derivative binding | 2 | 19 |
GO:1901265 | nucleoside phosphate binding | 3 | 19 |
GO:1901363 | heterocyclic compound binding | 2 | 19 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 401 | 405 | PF00656 | 0.393 |
CLV_C14_Caspase3-7 | 499 | 503 | PF00656 | 0.717 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.314 |
CLV_NRD_NRD_1 | 490 | 492 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 670 | 672 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.307 |
CLV_PCSK_KEX2_1 | 317 | 319 | PF00082 | 0.413 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 489 | 491 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 494 | 496 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.335 |
CLV_PCSK_PC1ET2_1 | 494 | 496 | PF00082 | 0.449 |
CLV_PCSK_PC7_1 | 417 | 423 | PF00082 | 0.322 |
CLV_PCSK_PC7_1 | 490 | 496 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 510 | 514 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.275 |
DEG_APCC_DBOX_1 | 525 | 533 | PF00400 | 0.518 |
DEG_APCC_DBOX_1 | 569 | 577 | PF00400 | 0.577 |
DOC_ANK_TNKS_1 | 319 | 326 | PF00023 | 0.562 |
DOC_CKS1_1 | 676 | 681 | PF01111 | 0.627 |
DOC_CYCLIN_RxL_1 | 507 | 514 | PF00134 | 0.554 |
DOC_CYCLIN_yClb1_LxF_4 | 327 | 332 | PF00134 | 0.528 |
DOC_CYCLIN_yCln2_LP_2 | 64 | 70 | PF00134 | 0.275 |
DOC_MAPK_gen_1 | 189 | 197 | PF00069 | 0.579 |
DOC_MAPK_gen_1 | 291 | 301 | PF00069 | 0.552 |
DOC_MAPK_gen_1 | 390 | 399 | PF00069 | 0.503 |
DOC_MAPK_gen_1 | 563 | 573 | PF00069 | 0.552 |
DOC_MAPK_gen_1 | 93 | 101 | PF00069 | 0.525 |
DOC_MAPK_MEF2A_6 | 355 | 362 | PF00069 | 0.474 |
DOC_MAPK_MEF2A_6 | 566 | 573 | PF00069 | 0.591 |
DOC_PIKK_1 | 110 | 118 | PF02985 | 0.525 |
DOC_PP1_RVXF_1 | 280 | 286 | PF00149 | 0.588 |
DOC_PP1_RVXF_1 | 327 | 333 | PF00149 | 0.527 |
DOC_PP2B_LxvP_1 | 540 | 543 | PF13499 | 0.481 |
DOC_PP2B_LxvP_1 | 64 | 67 | PF13499 | 0.335 |
DOC_SPAK_OSR1_1 | 320 | 324 | PF12202 | 0.570 |
DOC_SPAK_OSR1_1 | 566 | 570 | PF12202 | 0.618 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.397 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.496 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.444 |
DOC_WW_Pin1_4 | 592 | 597 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 675 | 680 | PF00397 | 0.544 |
LIG_14-3-3_CanoR_1 | 228 | 234 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 355 | 361 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 426 | 433 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 489 | 498 | PF00244 | 0.735 |
LIG_14-3-3_CanoR_1 | 566 | 570 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 6 | 12 | PF00244 | 0.443 |
LIG_AP2alpha_2 | 224 | 226 | PF02296 | 0.462 |
LIG_APCC_ABBA_1 | 106 | 111 | PF00400 | 0.559 |
LIG_APCC_ABBA_1 | 253 | 258 | PF00400 | 0.572 |
LIG_APCC_ABBA_1 | 397 | 402 | PF00400 | 0.481 |
LIG_BIR_III_4 | 541 | 545 | PF00653 | 0.458 |
LIG_deltaCOP1_diTrp_1 | 52 | 61 | PF00928 | 0.470 |
LIG_EH1_1 | 512 | 520 | PF00400 | 0.543 |
LIG_eIF4E_1 | 95 | 101 | PF01652 | 0.489 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.536 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.674 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.431 |
LIG_FHA_2 | 497 | 503 | PF00498 | 0.593 |
LIG_FHA_2 | 676 | 682 | PF00498 | 0.604 |
LIG_LIR_Apic_2 | 160 | 166 | PF02991 | 0.617 |
LIG_LIR_Apic_2 | 52 | 56 | PF02991 | 0.467 |
LIG_LIR_Apic_2 | 555 | 559 | PF02991 | 0.570 |
LIG_LIR_Gen_1 | 19 | 30 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 574 | 582 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 60 | 69 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 153 | 158 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 19 | 25 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 198 | 203 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 52 | 57 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 60 | 64 | PF02991 | 0.324 |
LIG_NRBOX | 528 | 534 | PF00104 | 0.531 |
LIG_PCNA_PIPBox_1 | 689 | 698 | PF02747 | 0.548 |
LIG_PCNA_TLS_4 | 194 | 201 | PF02747 | 0.471 |
LIG_PCNA_yPIPBox_3 | 689 | 701 | PF02747 | 0.449 |
LIG_PDZ_Class_3 | 704 | 709 | PF00595 | 0.505 |
LIG_Pex14_1 | 271 | 275 | PF04695 | 0.538 |
LIG_Pex14_2 | 296 | 300 | PF04695 | 0.527 |
LIG_Pex14_2 | 376 | 380 | PF04695 | 0.529 |
LIG_Pex14_2 | 57 | 61 | PF04695 | 0.447 |
LIG_Rb_pABgroove_1 | 394 | 402 | PF01858 | 0.481 |
LIG_REV1ctd_RIR_1 | 373 | 382 | PF16727 | 0.460 |
LIG_SH2_CRK | 163 | 167 | PF00017 | 0.596 |
LIG_SH2_CRK | 335 | 339 | PF00017 | 0.468 |
LIG_SH2_GRB2like | 284 | 287 | PF00017 | 0.440 |
LIG_SH2_NCK_1 | 109 | 113 | PF00017 | 0.558 |
LIG_SH2_NCK_1 | 163 | 167 | PF00017 | 0.586 |
LIG_SH2_SRC | 109 | 112 | PF00017 | 0.613 |
LIG_SH2_SRC | 171 | 174 | PF00017 | 0.700 |
LIG_SH2_SRC | 200 | 203 | PF00017 | 0.469 |
LIG_SH2_STAP1 | 372 | 376 | PF00017 | 0.468 |
LIG_SH2_STAP1 | 95 | 99 | PF00017 | 0.648 |
LIG_SH2_STAT3 | 284 | 287 | PF00017 | 0.440 |
LIG_SH2_STAT3 | 673 | 676 | PF00017 | 0.592 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.590 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 673 | 676 | PF00017 | 0.493 |
LIG_SH3_1 | 53 | 59 | PF00018 | 0.356 |
LIG_SH3_3 | 331 | 337 | PF00018 | 0.481 |
LIG_SH3_3 | 355 | 361 | PF00018 | 0.544 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.356 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.283 |
LIG_SUMO_SIM_anti_2 | 307 | 312 | PF11976 | 0.527 |
LIG_SUMO_SIM_anti_2 | 60 | 66 | PF11976 | 0.280 |
LIG_SUMO_SIM_par_1 | 305 | 312 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 546 | 552 | PF11976 | 0.533 |
LIG_TRAF2_1 | 650 | 653 | PF00917 | 0.548 |
LIG_TYR_ITIM | 587 | 592 | PF00017 | 0.445 |
MOD_CDC14_SPxK_1 | 165 | 168 | PF00782 | 0.438 |
MOD_CDK_SPK_2 | 592 | 597 | PF00069 | 0.430 |
MOD_CDK_SPxK_1 | 162 | 168 | PF00069 | 0.450 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.573 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.382 |
MOD_CK2_1 | 479 | 485 | PF00069 | 0.602 |
MOD_CK2_1 | 675 | 681 | PF00069 | 0.404 |
MOD_Cter_Amidation | 91 | 94 | PF01082 | 0.375 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.617 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.409 |
MOD_GlcNHglycan | 457 | 461 | PF01048 | 0.582 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.391 |
MOD_GlcNHglycan | 611 | 614 | PF01048 | 0.687 |
MOD_GlcNHglycan | 666 | 670 | PF01048 | 0.696 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.514 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.541 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.732 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.676 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.433 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.559 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.734 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.611 |
MOD_N-GLC_1 | 14 | 19 | PF02516 | 0.472 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.585 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.713 |
MOD_NEK2_2 | 213 | 218 | PF00069 | 0.537 |
MOD_NEK2_2 | 295 | 300 | PF00069 | 0.438 |
MOD_NEK2_2 | 565 | 570 | PF00069 | 0.445 |
MOD_PIKK_1 | 137 | 143 | PF00454 | 0.495 |
MOD_PIKK_1 | 694 | 700 | PF00454 | 0.406 |
MOD_PKA_1 | 219 | 225 | PF00069 | 0.429 |
MOD_PKA_1 | 489 | 495 | PF00069 | 0.693 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.537 |
MOD_PKA_2 | 489 | 495 | PF00069 | 0.633 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.552 |
MOD_PKA_2 | 565 | 571 | PF00069 | 0.470 |
MOD_PKA_2 | 703 | 709 | PF00069 | 0.559 |
MOD_Plk_1 | 183 | 189 | PF00069 | 0.421 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.476 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.425 |
MOD_Plk_1 | 304 | 310 | PF00069 | 0.511 |
MOD_Plk_1 | 456 | 462 | PF00069 | 0.520 |
MOD_Plk_2-3 | 379 | 385 | PF00069 | 0.268 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.420 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.389 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.386 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.519 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.625 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.498 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.709 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.548 |
MOD_ProDKin_1 | 592 | 598 | PF00069 | 0.455 |
MOD_ProDKin_1 | 675 | 681 | PF00069 | 0.415 |
MOD_SUMO_for_1 | 182 | 185 | PF00179 | 0.464 |
MOD_SUMO_rev_2 | 278 | 283 | PF00179 | 0.514 |
TRG_DiLeu_BaEn_1 | 577 | 582 | PF01217 | 0.510 |
TRG_DiLeu_BaEn_1 | 60 | 65 | PF01217 | 0.341 |
TRG_DiLeu_BaEn_2 | 393 | 399 | PF01217 | 0.333 |
TRG_DiLeu_BaLyEn_6 | 35 | 40 | PF01217 | 0.440 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.557 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 372 | 375 | PF00928 | 0.290 |
TRG_ENDOCYTIC_2 | 575 | 578 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 589 | 592 | PF00928 | 0.457 |
TRG_ER_diArg_1 | 189 | 192 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 317 | 320 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 489 | 491 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 569 | 572 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 93 | 95 | PF00400 | 0.363 |
TRG_NES_CRM1_1 | 577 | 591 | PF08389 | 0.402 |
TRG_Pf-PMV_PEXEL_1 | 510 | 514 | PF00026 | 0.424 |
TRG_Pf-PMV_PEXEL_1 | 634 | 638 | PF00026 | 0.461 |
TRG_Pf-PMV_PEXEL_1 | 98 | 103 | PF00026 | 0.329 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P906 | Leptomonas seymouri | 28% | 96% |
A0A0S4JAD3 | Bodo saltans | 32% | 100% |
A0A1X0NTT2 | Trypanosomatidae | 37% | 100% |
A0A3Q8IC80 | Leishmania donovani | 75% | 96% |
A0A3Q8IC95 | Leishmania donovani | 64% | 98% |
A0A3Q8IHZ0 | Leishmania donovani | 28% | 99% |
A0A422NUH1 | Trypanosoma rangeli | 34% | 100% |
A4HZW7 | Leishmania infantum | 65% | 99% |
A4IDZ9 | Leishmania infantum | 27% | 99% |
C9ZSJ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AU21 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 99% |
E9AVS5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 60% | 98% |
E9AVS6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 97% |
Q4Q0H4 | Leishmania major | 27% | 97% |
Q4QBQ3 | Leishmania major | 75% | 100% |
Q4QBQ4 | Leishmania major | 65% | 100% |
V5DMJ8 | Trypanosoma cruzi | 35% | 98% |