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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A0A3S7X5E9
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 11 |
GO:0006793 | phosphorus metabolic process | 3 | 11 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016310 | phosphorylation | 5 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0036211 | protein modification process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004672 | protein kinase activity | 3 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016301 | kinase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 11 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 145 | 149 | PF00656 | 0.651 |
CLV_C14_Caspase3-7 | 324 | 328 | PF00656 | 0.591 |
CLV_C14_Caspase3-7 | 466 | 470 | PF00656 | 0.562 |
CLV_C14_Caspase3-7 | 47 | 51 | PF00656 | 0.581 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.357 |
CLV_NRD_NRD_1 | 498 | 500 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 545 | 547 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 563 | 565 | PF00675 | 0.555 |
CLV_PCSK_FUR_1 | 561 | 565 | PF00082 | 0.381 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 498 | 500 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 505 | 507 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 545 | 547 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 563 | 565 | PF00082 | 0.570 |
CLV_PCSK_PC1ET2_1 | 505 | 507 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 511 | 515 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.485 |
CLV_Separin_Metazoa | 528 | 532 | PF03568 | 0.487 |
DEG_SCF_FBW7_1 | 408 | 415 | PF00400 | 0.410 |
DEG_SPOP_SBC_1 | 140 | 144 | PF00917 | 0.614 |
DEG_SPOP_SBC_1 | 326 | 330 | PF00917 | 0.588 |
DEG_SPOP_SBC_1 | 335 | 339 | PF00917 | 0.445 |
DOC_CKS1_1 | 251 | 256 | PF01111 | 0.468 |
DOC_CYCLIN_yCln2_LP_2 | 296 | 302 | PF00134 | 0.362 |
DOC_CYCLIN_yCln2_LP_2 | 76 | 79 | PF00134 | 0.564 |
DOC_MAPK_gen_1 | 274 | 284 | PF00069 | 0.377 |
DOC_MAPK_MEF2A_6 | 274 | 282 | PF00069 | 0.405 |
DOC_MAPK_MEF2A_6 | 490 | 497 | PF00069 | 0.543 |
DOC_PP1_RVXF_1 | 479 | 486 | PF00149 | 0.548 |
DOC_PP2B_LxvP_1 | 264 | 267 | PF13499 | 0.350 |
DOC_PP2B_LxvP_1 | 280 | 283 | PF13499 | 0.461 |
DOC_PP2B_LxvP_1 | 76 | 79 | PF13499 | 0.564 |
DOC_PP4_FxxP_1 | 251 | 254 | PF00568 | 0.532 |
DOC_PP4_FxxP_1 | 80 | 83 | PF00568 | 0.746 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.381 |
DOC_USP7_UBL2_3 | 213 | 217 | PF12436 | 0.442 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.349 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.306 |
LIG_14-3-3_CanoR_1 | 208 | 216 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 243 | 252 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 341 | 347 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 531 | 536 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 94 | 102 | PF00244 | 0.552 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.624 |
LIG_BRCT_BRCA1_1 | 2 | 6 | PF00533 | 0.674 |
LIG_BRCT_BRCA1_1 | 247 | 251 | PF00533 | 0.604 |
LIG_BRCT_BRCA1_1 | 336 | 340 | PF00533 | 0.480 |
LIG_deltaCOP1_diTrp_1 | 440 | 444 | PF00928 | 0.426 |
LIG_eIF4E_1 | 259 | 265 | PF01652 | 0.474 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.356 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.503 |
LIG_FHA_1 | 550 | 556 | PF00498 | 0.456 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.503 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.635 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.735 |
LIG_FHA_2 | 251 | 257 | PF00498 | 0.519 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.297 |
LIG_FHA_2 | 451 | 457 | PF00498 | 0.279 |
LIG_FHA_2 | 552 | 558 | PF00498 | 0.417 |
LIG_LIR_Apic_2 | 248 | 254 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 121 | 130 | PF02991 | 0.745 |
LIG_LIR_Gen_1 | 256 | 267 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 404 | 412 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 121 | 125 | PF02991 | 0.745 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 256 | 262 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 343 | 349 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 404 | 408 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 538 | 544 | PF02991 | 0.383 |
LIG_MYND_1 | 250 | 254 | PF01753 | 0.542 |
LIG_PCNA_TLS_4 | 105 | 112 | PF02747 | 0.440 |
LIG_RPA_C_Fungi | 494 | 506 | PF08784 | 0.372 |
LIG_SH2_CRK | 259 | 263 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.697 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.482 |
LIG_SH3_3 | 179 | 185 | PF00018 | 0.535 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.580 |
LIG_SUMO_SIM_par_1 | 447 | 453 | PF11976 | 0.281 |
LIG_TRAF2_1 | 253 | 256 | PF00917 | 0.548 |
LIG_UBA3_1 | 513 | 519 | PF00899 | 0.324 |
MOD_CDK_SPxK_1 | 410 | 416 | PF00069 | 0.355 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.701 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.639 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.659 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.501 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.593 |
MOD_CK1_1 | 342 | 348 | PF00069 | 0.353 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.429 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.410 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.714 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.285 |
MOD_CK1_1 | 549 | 555 | PF00069 | 0.360 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.504 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.631 |
MOD_CK2_1 | 120 | 126 | PF00069 | 0.608 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.560 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.402 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.574 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.457 |
MOD_CK2_1 | 531 | 537 | PF00069 | 0.444 |
MOD_CK2_1 | 551 | 557 | PF00069 | 0.526 |
MOD_Cter_Amidation | 503 | 506 | PF01082 | 0.428 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.673 |
MOD_GlcNHglycan | 121 | 125 | PF01048 | 0.641 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.717 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.482 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.666 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.675 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.694 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.600 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.497 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.576 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.681 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.501 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.413 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.633 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.351 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.404 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.684 |
MOD_N-GLC_1 | 132 | 137 | PF02516 | 0.739 |
MOD_N-GLC_1 | 285 | 290 | PF02516 | 0.481 |
MOD_N-GLC_2 | 132 | 134 | PF02516 | 0.694 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.563 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.581 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.498 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.732 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.418 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.387 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.441 |
MOD_NEK2_2 | 285 | 290 | PF00069 | 0.474 |
MOD_NEK2_2 | 551 | 556 | PF00069 | 0.463 |
MOD_PIKK_1 | 28 | 34 | PF00454 | 0.471 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.400 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.523 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.521 |
MOD_PKA_2 | 477 | 483 | PF00069 | 0.542 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.614 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.699 |
MOD_PKB_1 | 241 | 249 | PF00069 | 0.497 |
MOD_PKB_1 | 40 | 48 | PF00069 | 0.471 |
MOD_Plk_1 | 120 | 126 | PF00069 | 0.542 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.570 |
MOD_Plk_1 | 226 | 232 | PF00069 | 0.454 |
MOD_Plk_1 | 285 | 291 | PF00069 | 0.398 |
MOD_Plk_1 | 546 | 552 | PF00069 | 0.371 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.373 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.717 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.480 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.288 |
MOD_Plk_4 | 531 | 537 | PF00069 | 0.511 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.641 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.623 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.349 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.298 |
MOD_SUMO_rev_2 | 205 | 215 | PF00179 | 0.511 |
TRG_DiLeu_BaEn_1 | 276 | 281 | PF01217 | 0.412 |
TRG_DiLeu_BaEn_1 | 509 | 514 | PF01217 | 0.476 |
TRG_DiLeu_BaEn_2 | 363 | 369 | PF01217 | 0.355 |
TRG_DiLeu_BaEn_2 | 536 | 542 | PF01217 | 0.413 |
TRG_DiLeu_BaEn_4 | 537 | 543 | PF01217 | 0.396 |
TRG_DiLeu_BaLyEn_6 | 468 | 473 | PF01217 | 0.501 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.595 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 346 | 349 | PF00928 | 0.478 |
TRG_ER_diArg_1 | 420 | 422 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 497 | 499 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 544 | 546 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 561 | 564 | PF00400 | 0.417 |
TRG_Pf-PMV_PEXEL_1 | 481 | 486 | PF00026 | 0.528 |
TRG_Pf-PMV_PEXEL_1 | 505 | 509 | PF00026 | 0.417 |
TRG_Pf-PMV_PEXEL_1 | 511 | 515 | PF00026 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 82 | 86 | PF00026 | 0.669 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEH1 | Leptomonas seymouri | 66% | 100% |
A0A1X0NUL0 | Trypanosomatidae | 38% | 100% |
A0A422P1A6 | Trypanosoma rangeli | 39% | 100% |
A4HKB7 | Leishmania braziliensis | 73% | 99% |
A4I7U6 | Leishmania infantum | 97% | 98% |
D0AA04 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9B2Q4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q5F3 | Leishmania major | 93% | 100% |
V5BGP5 | Trypanosoma cruzi | 40% | 100% |