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: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4QHV9
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 5 |
GO:0003824 | catalytic activity | 1 | 5 |
GO:0005488 | binding | 1 | 5 |
GO:0005524 | ATP binding | 5 | 5 |
GO:0016301 | kinase activity | 4 | 5 |
GO:0016740 | transferase activity | 2 | 5 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 5 |
GO:0017076 | purine nucleotide binding | 4 | 5 |
GO:0030554 | adenyl nucleotide binding | 5 | 5 |
GO:0032553 | ribonucleotide binding | 3 | 5 |
GO:0032555 | purine ribonucleotide binding | 4 | 5 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 5 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 5 |
GO:0036094 | small molecule binding | 2 | 5 |
GO:0043167 | ion binding | 2 | 5 |
GO:0043168 | anion binding | 3 | 5 |
GO:0097159 | organic cyclic compound binding | 2 | 5 |
GO:0097367 | carbohydrate derivative binding | 2 | 5 |
GO:1901265 | nucleoside phosphate binding | 3 | 5 |
GO:1901363 | heterocyclic compound binding | 2 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 462 | 464 | PF00675 | 0.666 |
CLV_NRD_NRD_1 | 465 | 467 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 581 | 583 | PF00675 | 0.676 |
CLV_PCSK_FUR_1 | 460 | 464 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 462 | 464 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 465 | 467 | PF00082 | 0.694 |
CLV_PCSK_KEX2_1 | 581 | 583 | PF00082 | 0.676 |
CLV_PCSK_PC1ET2_1 | 331 | 333 | PF00082 | 0.439 |
CLV_PCSK_PC7_1 | 308 | 314 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 410 | 414 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 466 | 470 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.627 |
CLV_PCSK_SKI1_1 | 582 | 586 | PF00082 | 0.669 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.554 |
DEG_APCC_DBOX_1 | 60 | 68 | PF00400 | 0.573 |
DEG_COP1_1 | 9 | 18 | PF00400 | 0.753 |
DEG_SCF_FBW7_1 | 112 | 119 | PF00400 | 0.796 |
DOC_CKS1_1 | 15 | 20 | PF01111 | 0.719 |
DOC_CYCLIN_RxL_1 | 532 | 539 | PF00134 | 0.644 |
DOC_CYCLIN_yCln2_LP_2 | 100 | 106 | PF00134 | 0.674 |
DOC_CYCLIN_yCln2_LP_2 | 124 | 130 | PF00134 | 0.649 |
DOC_MAPK_DCC_7 | 122 | 132 | PF00069 | 0.656 |
DOC_MAPK_gen_1 | 312 | 318 | PF00069 | 0.461 |
DOC_MAPK_gen_1 | 331 | 337 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 449 | 458 | PF00069 | 0.563 |
DOC_MAPK_gen_1 | 523 | 532 | PF00069 | 0.677 |
DOC_MAPK_MEF2A_6 | 122 | 130 | PF00069 | 0.672 |
DOC_MAPK_MEF2A_6 | 196 | 203 | PF00069 | 0.511 |
DOC_MAPK_MEF2A_6 | 339 | 347 | PF00069 | 0.431 |
DOC_MAPK_RevD_3 | 297 | 313 | PF00069 | 0.473 |
DOC_MAPK_RevD_3 | 316 | 332 | PF00069 | 0.445 |
DOC_PP2B_LxvP_1 | 124 | 127 | PF13499 | 0.666 |
DOC_PP2B_LxvP_1 | 154 | 157 | PF13499 | 0.487 |
DOC_PP2B_LxvP_1 | 222 | 225 | PF13499 | 0.513 |
DOC_PP2B_LxvP_1 | 612 | 615 | PF13499 | 0.571 |
DOC_PP4_FxxP_1 | 117 | 120 | PF00568 | 0.724 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.216 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 587 | 591 | PF00917 | 0.691 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.759 |
DOC_WW_Pin1_4 | 509 | 514 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.683 |
LIG_14-3-3_CanoR_1 | 364 | 369 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 40 | 49 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 463 | 473 | PF00244 | 0.617 |
LIG_14-3-3_CanoR_1 | 523 | 532 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 581 | 585 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 77 | 86 | PF00244 | 0.569 |
LIG_BRCT_BRCA1_1 | 113 | 117 | PF00533 | 0.678 |
LIG_BRCT_BRCA1_1 | 570 | 574 | PF00533 | 0.677 |
LIG_FAT_LD_1 | 302 | 310 | PF03623 | 0.444 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.353 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.411 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.584 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.588 |
LIG_FHA_2 | 260 | 266 | PF00498 | 0.580 |
LIG_FHA_2 | 404 | 410 | PF00498 | 0.554 |
LIG_FHA_2 | 416 | 422 | PF00498 | 0.477 |
LIG_HP1_1 | 103 | 107 | PF01393 | 0.655 |
LIG_LIR_Apic_2 | 114 | 120 | PF02991 | 0.720 |
LIG_LIR_Gen_1 | 184 | 191 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 409 | 420 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 422 | 433 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 494 | 504 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 607 | 617 | PF02991 | 0.651 |
LIG_LIR_Nem_3 | 184 | 189 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 245 | 251 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 29 | 34 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 378 | 382 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 409 | 415 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 422 | 428 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 494 | 500 | PF02991 | 0.683 |
LIG_LIR_Nem_3 | 57 | 62 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 607 | 612 | PF02991 | 0.663 |
LIG_NRBOX | 305 | 311 | PF00104 | 0.494 |
LIG_NRBOX | 85 | 91 | PF00104 | 0.585 |
LIG_OCRL_FandH_1 | 411 | 423 | PF00620 | 0.507 |
LIG_Pex14_2 | 248 | 252 | PF04695 | 0.509 |
LIG_RPA_C_Plants | 369 | 380 | PF08784 | 0.535 |
LIG_SH2_CRK | 425 | 429 | PF00017 | 0.511 |
LIG_SH2_NCK_1 | 94 | 98 | PF00017 | 0.569 |
LIG_SH2_STAP1 | 94 | 98 | PF00017 | 0.607 |
LIG_SH2_STAT3 | 291 | 294 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.630 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.810 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.662 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.447 |
LIG_SH3_3 | 498 | 504 | PF00018 | 0.708 |
LIG_SH3_3 | 507 | 513 | PF00018 | 0.584 |
LIG_SUMO_SIM_par_1 | 101 | 111 | PF11976 | 0.691 |
LIG_SUMO_SIM_par_1 | 128 | 134 | PF11976 | 0.614 |
LIG_SUMO_SIM_par_1 | 397 | 404 | PF11976 | 0.492 |
LIG_WRC_WIRS_1 | 376 | 381 | PF05994 | 0.494 |
MOD_CDC14_SPxK_1 | 119 | 122 | PF00782 | 0.663 |
MOD_CDK_SPxK_1 | 112 | 118 | PF00069 | 0.719 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.661 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.513 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.553 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.767 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.724 |
MOD_CK1_1 | 546 | 552 | PF00069 | 0.711 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.562 |
MOD_CK1_1 | 590 | 596 | PF00069 | 0.796 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.761 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.661 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.485 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.564 |
MOD_CK2_1 | 351 | 357 | PF00069 | 0.516 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.580 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.788 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.627 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.474 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.339 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.766 |
MOD_GlcNHglycan | 272 | 276 | PF01048 | 0.719 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.529 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.732 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.504 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.798 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.730 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.595 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.687 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.696 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.557 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.667 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.591 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.403 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.530 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.670 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.493 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.716 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.630 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.824 |
MOD_GSK3_1 | 554 | 561 | PF00069 | 0.720 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.660 |
MOD_GSK3_1 | 613 | 620 | PF00069 | 0.650 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.514 |
MOD_N-GLC_1 | 471 | 476 | PF02516 | 0.713 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.786 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.570 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.411 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.482 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.567 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.491 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.519 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.474 |
MOD_NEK2_1 | 594 | 599 | PF00069 | 0.796 |
MOD_NEK2_2 | 375 | 380 | PF00069 | 0.568 |
MOD_PIKK_1 | 144 | 150 | PF00454 | 0.738 |
MOD_PIKK_1 | 217 | 223 | PF00454 | 0.411 |
MOD_PK_1 | 312 | 318 | PF00069 | 0.461 |
MOD_PKA_1 | 312 | 318 | PF00069 | 0.461 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.461 |
MOD_PKA_2 | 464 | 470 | PF00069 | 0.648 |
MOD_PKA_2 | 546 | 552 | PF00069 | 0.711 |
MOD_PKA_2 | 580 | 586 | PF00069 | 0.765 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.591 |
MOD_PKB_1 | 362 | 370 | PF00069 | 0.600 |
MOD_Plk_1 | 408 | 414 | PF00069 | 0.493 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.436 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.502 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.461 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.510 |
MOD_Plk_4 | 554 | 560 | PF00069 | 0.808 |
MOD_Plk_4 | 613 | 619 | PF00069 | 0.767 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.710 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.675 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.586 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.765 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.767 |
MOD_ProDKin_1 | 509 | 515 | PF00069 | 0.761 |
MOD_SUMO_rev_2 | 139 | 147 | PF00179 | 0.514 |
TRG_DiLeu_BaEn_1 | 319 | 324 | PF01217 | 0.440 |
TRG_DiLeu_BaEn_1 | 613 | 618 | PF01217 | 0.769 |
TRG_DiLeu_BaEn_4 | 607 | 613 | PF01217 | 0.564 |
TRG_DiLeu_BaLyEn_6 | 305 | 310 | PF01217 | 0.469 |
TRG_DiLeu_BaLyEn_6 | 33 | 38 | PF01217 | 0.574 |
TRG_ENDOCYTIC_2 | 425 | 428 | PF00928 | 0.544 |
TRG_ER_diArg_1 | 237 | 240 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 361 | 364 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 459 | 462 | PF00400 | 0.638 |
TRG_ER_diArg_1 | 464 | 466 | PF00400 | 0.671 |
TRG_ER_diArg_1 | 522 | 525 | PF00400 | 0.730 |
TRG_ER_diArg_1 | 580 | 582 | PF00400 | 0.735 |
TRG_Pf-PMV_PEXEL_1 | 535 | 539 | PF00026 | 0.553 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I622 | Leptomonas seymouri | 48% | 93% |
A0A3S5H6D7 | Leishmania donovani | 90% | 97% |
A4H5P6 | Leishmania braziliensis | 77% | 97% |
A4HTY6 | Leishmania infantum | 91% | 97% |
E9AMR6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 97% |