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: E9B6G6
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016310 | phosphorylation | 5 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0036211 | protein modification process | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004672 | protein kinase activity | 3 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0016301 | kinase activity | 4 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 7 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 112 | 116 | PF00656 | 0.573 |
CLV_C14_Caspase3-7 | 162 | 166 | PF00656 | 0.544 |
CLV_C14_Caspase3-7 | 194 | 198 | PF00656 | 0.435 |
CLV_C14_Caspase3-7 | 203 | 207 | PF00656 | 0.427 |
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 444 | 446 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 727 | 729 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 730 | 732 | PF00675 | 0.523 |
CLV_PCSK_FUR_1 | 100 | 104 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.527 |
CLV_PCSK_PC1ET2_1 | 210 | 212 | PF00082 | 0.412 |
CLV_PCSK_PC1ET2_1 | 405 | 407 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 596 | 600 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 733 | 737 | PF00082 | 0.590 |
DEG_APCC_DBOX_1 | 265 | 273 | PF00400 | 0.367 |
DEG_COP1_1 | 678 | 688 | PF00400 | 0.509 |
DEG_SCF_FBW7_2 | 75 | 82 | PF00400 | 0.470 |
DEG_SPOP_SBC_1 | 126 | 130 | PF00917 | 0.626 |
DEG_SPOP_SBC_1 | 146 | 150 | PF00917 | 0.510 |
DEG_SPOP_SBC_1 | 181 | 185 | PF00917 | 0.485 |
DEG_SPOP_SBC_1 | 716 | 720 | PF00917 | 0.551 |
DOC_CKS1_1 | 489 | 494 | PF01111 | 0.619 |
DOC_CKS1_1 | 76 | 81 | PF01111 | 0.475 |
DOC_CYCLIN_yCln2_LP_2 | 376 | 382 | PF00134 | 0.455 |
DOC_MAPK_gen_1 | 210 | 220 | PF00069 | 0.384 |
DOC_MAPK_gen_1 | 614 | 624 | PF00069 | 0.378 |
DOC_MAPK_gen_1 | 9 | 19 | PF00069 | 0.428 |
DOC_MAPK_MEF2A_6 | 260 | 269 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 617 | 624 | PF00069 | 0.384 |
DOC_MAPK_RevD_3 | 90 | 103 | PF00069 | 0.613 |
DOC_MIT_MIM_1 | 619 | 629 | PF04212 | 0.554 |
DOC_PP1_RVXF_1 | 619 | 625 | PF00149 | 0.495 |
DOC_PP2B_LxvP_1 | 328 | 331 | PF13499 | 0.490 |
DOC_PP2B_LxvP_1 | 41 | 44 | PF13499 | 0.499 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.399 |
DOC_USP7_MATH_1 | 516 | 520 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 572 | 576 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 716 | 720 | PF00917 | 0.644 |
DOC_USP7_UBL2_3 | 210 | 214 | PF12436 | 0.513 |
DOC_USP7_UBL2_3 | 59 | 63 | PF12436 | 0.480 |
DOC_USP7_UBL2_3 | 729 | 733 | PF12436 | 0.562 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.408 |
DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.511 |
LIG_14-3-3_CanoR_1 | 266 | 275 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 422 | 427 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 448 | 454 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 461 | 466 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 714 | 723 | PF00244 | 0.533 |
LIG_AP2alpha_1 | 495 | 499 | PF02296 | 0.613 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.548 |
LIG_BIR_III_2 | 667 | 671 | PF00653 | 0.510 |
LIG_Clathr_ClatBox_1 | 189 | 193 | PF01394 | 0.506 |
LIG_deltaCOP1_diTrp_1 | 486 | 495 | PF00928 | 0.508 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.539 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.612 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.700 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.617 |
LIG_FHA_1 | 589 | 595 | PF00498 | 0.591 |
LIG_FHA_1 | 599 | 605 | PF00498 | 0.483 |
LIG_FHA_1 | 643 | 649 | PF00498 | 0.428 |
LIG_FHA_1 | 696 | 702 | PF00498 | 0.626 |
LIG_FHA_1 | 716 | 722 | PF00498 | 0.408 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.621 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.570 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.624 |
LIG_FHA_2 | 423 | 429 | PF00498 | 0.504 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.574 |
LIG_GBD_Chelix_1 | 227 | 235 | PF00786 | 0.337 |
LIG_HCF-1_HBM_1 | 106 | 109 | PF13415 | 0.581 |
LIG_LIR_Apic_2 | 486 | 492 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 252 | 258 | PF02991 | 0.286 |
LIG_LIR_Gen_1 | 322 | 331 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 609 | 620 | PF02991 | 0.413 |
LIG_LIR_LC3C_4 | 187 | 191 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 25 | 29 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 322 | 327 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 494 | 498 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 556 | 561 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 609 | 615 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 72 | 76 | PF02991 | 0.531 |
LIG_PCNA_PIPBox_1 | 605 | 614 | PF02747 | 0.553 |
LIG_Pex14_2 | 495 | 499 | PF04695 | 0.613 |
LIG_PTAP_UEV_1 | 454 | 459 | PF05743 | 0.538 |
LIG_SH2_CRK | 26 | 30 | PF00017 | 0.535 |
LIG_SH2_GRB2like | 118 | 121 | PF00017 | 0.584 |
LIG_SH2_PTP2 | 73 | 76 | PF00017 | 0.529 |
LIG_SH2_SRC | 195 | 198 | PF00017 | 0.485 |
LIG_SH2_SRC | 204 | 207 | PF00017 | 0.323 |
LIG_SH2_STAP1 | 118 | 122 | PF00017 | 0.565 |
LIG_SH2_STAP1 | 204 | 208 | PF00017 | 0.366 |
LIG_SH2_STAT3 | 118 | 121 | PF00017 | 0.561 |
LIG_SH2_STAT3 | 36 | 39 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.591 |
LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.529 |
LIG_SH3_1 | 700 | 706 | PF00018 | 0.564 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.714 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.420 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.550 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.521 |
LIG_SH3_3 | 452 | 458 | PF00018 | 0.602 |
LIG_SH3_3 | 495 | 501 | PF00018 | 0.538 |
LIG_SH3_3 | 682 | 688 | PF00018 | 0.662 |
LIG_SH3_3 | 700 | 706 | PF00018 | 0.555 |
LIG_SUMO_SIM_anti_2 | 135 | 140 | PF11976 | 0.564 |
LIG_SUMO_SIM_anti_2 | 187 | 194 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 187 | 194 | PF11976 | 0.509 |
LIG_SUMO_SIM_par_1 | 47 | 54 | PF11976 | 0.496 |
LIG_SUMO_SIM_par_1 | 478 | 483 | PF11976 | 0.527 |
LIG_TRAF2_1 | 676 | 679 | PF00917 | 0.569 |
LIG_TRAF2_1 | 79 | 82 | PF00917 | 0.691 |
LIG_TRAF2_2 | 79 | 84 | PF00917 | 0.494 |
LIG_TYR_ITIM | 71 | 76 | PF00017 | 0.525 |
MOD_CDC14_SPxK_1 | 402 | 405 | PF00782 | 0.424 |
MOD_CDK_SPxK_1 | 399 | 405 | PF00069 | 0.412 |
MOD_CDK_SPxxK_3 | 399 | 406 | PF00069 | 0.405 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.670 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.576 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.695 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.523 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.579 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.524 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.514 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.532 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.313 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.574 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.660 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.462 |
MOD_CK2_1 | 422 | 428 | PF00069 | 0.513 |
MOD_CK2_1 | 681 | 687 | PF00069 | 0.612 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.610 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.622 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.630 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.690 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.484 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.581 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.517 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.463 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.381 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.581 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.562 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.540 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.616 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.551 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.614 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.639 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.759 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.597 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.617 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.388 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.610 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.707 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.624 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.572 |
MOD_GSK3_1 | 563 | 570 | PF00069 | 0.583 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.501 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.535 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.555 |
MOD_GSK3_1 | 655 | 662 | PF00069 | 0.486 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.686 |
MOD_LATS_1 | 459 | 465 | PF00433 | 0.656 |
MOD_N-GLC_1 | 357 | 362 | PF02516 | 0.467 |
MOD_N-GLC_1 | 363 | 368 | PF02516 | 0.439 |
MOD_N-GLC_1 | 429 | 434 | PF02516 | 0.347 |
MOD_N-GLC_1 | 55 | 60 | PF02516 | 0.609 |
MOD_N-GLC_1 | 716 | 721 | PF02516 | 0.562 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.570 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.469 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.633 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.553 |
MOD_NEK2_1 | 655 | 660 | PF00069 | 0.480 |
MOD_NEK2_1 | 722 | 727 | PF00069 | 0.592 |
MOD_PIKK_1 | 563 | 569 | PF00454 | 0.545 |
MOD_PIKK_1 | 678 | 684 | PF00454 | 0.580 |
MOD_PK_1 | 405 | 411 | PF00069 | 0.304 |
MOD_PKA_1 | 405 | 411 | PF00069 | 0.405 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.565 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.405 |
MOD_Plk_1 | 429 | 435 | PF00069 | 0.335 |
MOD_Plk_1 | 475 | 481 | PF00069 | 0.559 |
MOD_Plk_1 | 716 | 722 | PF00069 | 0.564 |
MOD_Plk_2-3 | 197 | 203 | PF00069 | 0.381 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.648 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.487 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.449 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.446 |
MOD_Plk_4 | 408 | 414 | PF00069 | 0.420 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.425 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.684 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.552 |
MOD_Plk_4 | 600 | 606 | PF00069 | 0.506 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.552 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.546 |
MOD_Plk_4 | 717 | 723 | PF00069 | 0.590 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.661 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.629 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.584 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.412 |
MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.488 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.556 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.518 |
MOD_SUMO_rev_2 | 613 | 622 | PF00179 | 0.487 |
MOD_SUMO_rev_2 | 684 | 691 | PF00179 | 0.557 |
TRG_DiLeu_BaEn_2 | 307 | 313 | PF01217 | 0.539 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 558 | 561 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.529 |
TRG_ER_diArg_1 | 211 | 213 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 443 | 445 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 533 | 536 | PF00400 | 0.630 |
TRG_ER_diArg_1 | 99 | 102 | PF00400 | 0.555 |
TRG_NES_CRM1_1 | 640 | 652 | PF08389 | 0.507 |
TRG_NLS_MonoExtC_3 | 209 | 214 | PF00514 | 0.341 |
TRG_NLS_MonoExtC_3 | 727 | 732 | PF00514 | 0.581 |
TRG_NLS_MonoExtN_4 | 728 | 735 | PF00514 | 0.640 |
TRG_Pf-PMV_PEXEL_1 | 111 | 115 | PF00026 | 0.743 |
TRG_Pf-PMV_PEXEL_1 | 211 | 215 | PF00026 | 0.403 |
TRG_Pf-PMV_PEXEL_1 | 247 | 252 | PF00026 | 0.396 |
TRG_Pf-PMV_PEXEL_1 | 592 | 597 | PF00026 | 0.583 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFG5 | Leptomonas seymouri | 38% | 98% |
A0A3Q8IVC2 | Leishmania donovani | 81% | 100% |
A4HMV4 | Leishmania braziliensis | 61% | 100% |
A4IBH5 | Leishmania infantum | 81% | 100% |
E9AFB1 | Leishmania major | 82% | 100% |