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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: Q4Q9P0
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 10 |
GO:0006793 | phosphorus metabolic process | 3 | 10 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016310 | phosphorylation | 5 | 10 |
GO:0019538 | protein metabolic process | 3 | 10 |
GO:0036211 | protein modification process | 4 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043412 | macromolecule modification | 4 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004672 | protein kinase activity | 3 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0016301 | kinase activity | 4 | 10 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 10 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 256 | 260 | PF00656 | 0.551 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.679 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.785 |
CLV_NRD_NRD_1 | 503 | 505 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.298 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.264 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 503 | 505 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.180 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.629 |
DEG_APCC_DBOX_1 | 113 | 121 | PF00400 | 0.276 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.391 |
DEG_SPOP_SBC_1 | 239 | 243 | PF00917 | 0.469 |
DOC_ANK_TNKS_1 | 75 | 82 | PF00023 | 0.316 |
DOC_CDC14_PxL_1 | 433 | 441 | PF14671 | 0.591 |
DOC_CKS1_1 | 140 | 145 | PF01111 | 0.334 |
DOC_CKS1_1 | 160 | 165 | PF01111 | 0.218 |
DOC_CKS1_1 | 200 | 205 | PF01111 | 0.252 |
DOC_MAPK_gen_1 | 132 | 141 | PF00069 | 0.252 |
DOC_MAPK_gen_1 | 76 | 84 | PF00069 | 0.252 |
DOC_MAPK_MEF2A_6 | 76 | 84 | PF00069 | 0.252 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.395 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 512 | 516 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 522 | 526 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 540 | 544 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 554 | 558 | PF00917 | 0.614 |
DOC_USP7_UBL2_3 | 278 | 282 | PF12436 | 0.651 |
DOC_USP7_UBL2_3 | 6 | 10 | PF12436 | 0.276 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.381 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.227 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.187 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.269 |
DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 502 | 507 | PF00397 | 0.701 |
LIG_14-3-3_CanoR_1 | 171 | 177 | PF00244 | 0.185 |
LIG_14-3-3_CanoR_1 | 365 | 372 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 429 | 433 | PF00244 | 0.699 |
LIG_14-3-3_CanoR_1 | 481 | 489 | PF00244 | 0.682 |
LIG_14-3-3_CanoR_1 | 496 | 502 | PF00244 | 0.598 |
LIG_Actin_WH2_2 | 349 | 367 | PF00022 | 0.311 |
LIG_APCC_ABBA_1 | 165 | 170 | PF00400 | 0.174 |
LIG_BRCT_BRCA1_1 | 240 | 244 | PF00533 | 0.560 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.271 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.185 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.677 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.301 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.550 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.252 |
LIG_FHA_2 | 303 | 309 | PF00498 | 0.263 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.320 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.613 |
LIG_FHA_2 | 563 | 569 | PF00498 | 0.588 |
LIG_LIR_Apic_2 | 202 | 208 | PF02991 | 0.252 |
LIG_LIR_Apic_2 | 270 | 276 | PF02991 | 0.635 |
LIG_LIR_Apic_2 | 35 | 41 | PF02991 | 0.316 |
LIG_LIR_Gen_1 | 305 | 315 | PF02991 | 0.252 |
LIG_LIR_Gen_1 | 352 | 360 | PF02991 | 0.287 |
LIG_LIR_Gen_1 | 525 | 535 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 568 | 576 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 305 | 310 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 352 | 356 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 431 | 436 | PF02991 | 0.652 |
LIG_LIR_Nem_3 | 525 | 531 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 568 | 572 | PF02991 | 0.541 |
LIG_MYND_1 | 375 | 379 | PF01753 | 0.431 |
LIG_Pex14_2 | 244 | 248 | PF04695 | 0.561 |
LIG_SH2_CRK | 274 | 278 | PF00017 | 0.617 |
LIG_SH2_CRK | 528 | 532 | PF00017 | 0.487 |
LIG_SH2_GRB2like | 273 | 276 | PF00017 | 0.627 |
LIG_SH2_NCK_1 | 307 | 311 | PF00017 | 0.330 |
LIG_SH2_STAP1 | 112 | 116 | PF00017 | 0.252 |
LIG_SH2_STAP1 | 293 | 297 | PF00017 | 0.252 |
LIG_SH2_STAP1 | 360 | 364 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.263 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.235 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.252 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.276 |
LIG_SH3_1 | 38 | 44 | PF00018 | 0.185 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.391 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.252 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.253 |
LIG_SH3_3 | 38 | 44 | PF00018 | 0.274 |
LIG_SH3_3 | 442 | 448 | PF00018 | 0.619 |
LIG_SH3_3 | 450 | 456 | PF00018 | 0.590 |
LIG_SH3_4 | 396 | 403 | PF00018 | 0.547 |
LIG_SUMO_SIM_par_1 | 551 | 558 | PF11976 | 0.481 |
LIG_TYR_ITSM | 303 | 310 | PF00017 | 0.311 |
LIG_WRC_WIRS_1 | 350 | 355 | PF05994 | 0.381 |
LIG_WW_1 | 265 | 268 | PF00397 | 0.663 |
MOD_CDC14_SPxK_1 | 478 | 481 | PF00782 | 0.598 |
MOD_CDK_SPxK_1 | 475 | 481 | PF00069 | 0.593 |
MOD_CDK_SPxxK_3 | 139 | 146 | PF00069 | 0.369 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.543 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.599 |
MOD_CK1_1 | 497 | 503 | PF00069 | 0.720 |
MOD_CK1_1 | 505 | 511 | PF00069 | 0.640 |
MOD_CK1_1 | 514 | 520 | PF00069 | 0.566 |
MOD_CK1_1 | 543 | 549 | PF00069 | 0.691 |
MOD_CK1_1 | 558 | 564 | PF00069 | 0.608 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.369 |
MOD_CK2_1 | 240 | 246 | PF00069 | 0.679 |
MOD_CK2_1 | 302 | 308 | PF00069 | 0.252 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.285 |
MOD_CK2_1 | 389 | 395 | PF00069 | 0.721 |
MOD_CK2_1 | 514 | 520 | PF00069 | 0.605 |
MOD_CK2_1 | 562 | 568 | PF00069 | 0.586 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.571 |
MOD_GlcNHglycan | 259 | 263 | PF01048 | 0.659 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.291 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.348 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.351 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.637 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.596 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.771 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.765 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.583 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.522 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.615 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.695 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.614 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.375 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.312 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.641 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.299 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.206 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.598 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.645 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.725 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.704 |
MOD_GSK3_1 | 554 | 561 | PF00069 | 0.712 |
MOD_N-GLC_1 | 239 | 244 | PF02516 | 0.510 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.325 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.602 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.741 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.536 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.378 |
MOD_NEK2_1 | 489 | 494 | PF00069 | 0.749 |
MOD_NEK2_1 | 562 | 567 | PF00069 | 0.701 |
MOD_NEK2_2 | 428 | 433 | PF00069 | 0.558 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.276 |
MOD_PKA_2 | 428 | 434 | PF00069 | 0.588 |
MOD_PKA_2 | 482 | 488 | PF00069 | 0.682 |
MOD_PKA_2 | 538 | 544 | PF00069 | 0.623 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.470 |
MOD_Plk_2-3 | 349 | 355 | PF00069 | 0.280 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.615 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.258 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.347 |
MOD_Plk_4 | 558 | 564 | PF00069 | 0.555 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.381 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.227 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.187 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.670 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.269 |
MOD_ProDKin_1 | 452 | 458 | PF00069 | 0.596 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.593 |
MOD_ProDKin_1 | 502 | 508 | PF00069 | 0.700 |
MOD_SUMO_rev_2 | 390 | 397 | PF00179 | 0.536 |
TRG_DiLeu_BaEn_2 | 348 | 354 | PF01217 | 0.316 |
TRG_DiLeu_BaEn_2 | 567 | 573 | PF01217 | 0.552 |
TRG_DiLeu_BaLyEn_6 | 434 | 439 | PF01217 | 0.588 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.614 |
TRG_ENDOCYTIC_2 | 307 | 310 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.476 |
TRG_ER_diArg_1 | 185 | 188 | PF00400 | 0.372 |
TRG_ER_diArg_1 | 531 | 534 | PF00400 | 0.552 |
TRG_NES_CRM1_1 | 118 | 133 | PF08389 | 0.369 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8W2 | Leptomonas seymouri | 54% | 96% |
A0A1X0NYS1 | Trypanosomatidae | 40% | 100% |
A0A3S7WZA6 | Leishmania donovani | 93% | 100% |
A0A422P4L8 | Trypanosoma rangeli | 44% | 100% |
A4HEA1 | Leishmania braziliensis | 77% | 100% |
A4I1P7 | Leishmania infantum | 93% | 99% |
C9ZK98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AXT1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q1PFB9 | Arabidopsis thaliana | 24% | 100% |