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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4I5D1
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016310 | phosphorylation | 5 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0018105 | peptidyl-serine phosphorylation | 6 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018209 | peptidyl-serine modification | 6 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004672 | protein kinase activity | 3 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016301 | kinase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 2 |
GO:0106310 | protein serine kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 156 | 160 | PF00656 | 0.561 |
CLV_C14_Caspase3-7 | 269 | 273 | PF00656 | 0.688 |
CLV_C14_Caspase3-7 | 380 | 384 | PF00656 | 0.411 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.267 |
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 452 | 454 | PF00675 | 0.601 |
CLV_PCSK_FUR_1 | 290 | 294 | PF00082 | 0.568 |
CLV_PCSK_FUR_1 | 301 | 305 | PF00082 | 0.239 |
CLV_PCSK_FUR_1 | 450 | 454 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.199 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 452 | 454 | PF00082 | 0.601 |
CLV_PCSK_PC1ET2_1 | 174 | 176 | PF00082 | 0.289 |
CLV_PCSK_PC1ET2_1 | 412 | 414 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.244 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.344 |
DEG_COP1_1 | 153 | 161 | PF00400 | 0.412 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.599 |
DEG_SPOP_SBC_1 | 180 | 184 | PF00917 | 0.513 |
DEG_SPOP_SBC_1 | 285 | 289 | PF00917 | 0.498 |
DOC_CKS1_1 | 564 | 569 | PF01111 | 0.736 |
DOC_CYCLIN_RxL_1 | 184 | 193 | PF00134 | 0.513 |
DOC_MAPK_gen_1 | 216 | 225 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 228 | 236 | PF00069 | 0.444 |
DOC_MAPK_gen_1 | 290 | 296 | PF00069 | 0.552 |
DOC_MAPK_JIP1_4 | 20 | 26 | PF00069 | 0.512 |
DOC_MAPK_MEF2A_6 | 369 | 378 | PF00069 | 0.377 |
DOC_PP1_RVXF_1 | 185 | 192 | PF00149 | 0.486 |
DOC_PP4_FxxP_1 | 511 | 514 | PF00568 | 0.519 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.373 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 498 | 502 | PF00917 | 0.347 |
DOC_USP7_MATH_1 | 546 | 550 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 552 | 556 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 568 | 572 | PF00917 | 0.716 |
DOC_USP7_UBL2_3 | 58 | 62 | PF12436 | 0.444 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.313 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.430 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 563 | 568 | PF00397 | 0.670 |
LIG_14-3-3_CanoR_1 | 291 | 297 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 304 | 310 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 522 | 530 | PF00244 | 0.556 |
LIG_APCC_ABBA_1 | 414 | 419 | PF00400 | 0.489 |
LIG_APCC_ABBA_1 | 508 | 513 | PF00400 | 0.393 |
LIG_APCC_ABBAyCdc20_2 | 413 | 419 | PF00400 | 0.320 |
LIG_BIR_III_2 | 526 | 530 | PF00653 | 0.512 |
LIG_BIR_III_4 | 381 | 385 | PF00653 | 0.320 |
LIG_BIR_III_4 | 479 | 483 | PF00653 | 0.554 |
LIG_Clathr_ClatBox_1 | 233 | 237 | PF01394 | 0.444 |
LIG_deltaCOP1_diTrp_1 | 323 | 333 | PF00928 | 0.343 |
LIG_EH_1 | 527 | 531 | PF12763 | 0.477 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.412 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.446 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.514 |
LIG_FHA_1 | 564 | 570 | PF00498 | 0.723 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.374 |
LIG_FHA_2 | 533 | 539 | PF00498 | 0.605 |
LIG_FXI_DFP_1 | 233 | 237 | PF00024 | 0.244 |
LIG_LIR_Apic_2 | 312 | 318 | PF02991 | 0.283 |
LIG_LIR_Gen_1 | 190 | 199 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 353 | 362 | PF02991 | 0.321 |
LIG_LIR_Gen_1 | 392 | 402 | PF02991 | 0.258 |
LIG_LIR_Gen_1 | 504 | 514 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 101 | 107 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 190 | 194 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 353 | 358 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 371 | 376 | PF02991 | 0.247 |
LIG_LIR_Nem_3 | 392 | 398 | PF02991 | 0.258 |
LIG_LIR_Nem_3 | 504 | 509 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 513 | 519 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 601 | 607 | PF02991 | 0.535 |
LIG_PCNA_yPIPBox_3 | 62 | 75 | PF02747 | 0.544 |
LIG_Pex14_2 | 105 | 109 | PF04695 | 0.508 |
LIG_Pex14_2 | 530 | 534 | PF04695 | 0.652 |
LIG_SH2_CRK | 506 | 510 | PF00017 | 0.389 |
LIG_SH2_NCK_1 | 340 | 344 | PF00017 | 0.343 |
LIG_SH2_PTP2 | 315 | 318 | PF00017 | 0.299 |
LIG_SH2_STAP1 | 340 | 344 | PF00017 | 0.355 |
LIG_SH2_STAP1 | 516 | 520 | PF00017 | 0.421 |
LIG_SH2_STAT3 | 121 | 124 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 519 | 522 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 595 | 598 | PF00017 | 0.621 |
LIG_SH2_STAT5 | 603 | 606 | PF00017 | 0.661 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.494 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.565 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.555 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.491 |
LIG_SH3_3 | 561 | 567 | PF00018 | 0.719 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.611 |
LIG_SUMO_SIM_par_1 | 201 | 206 | PF11976 | 0.532 |
LIG_SxIP_EBH_1 | 174 | 185 | PF03271 | 0.508 |
LIG_TYR_ITIM | 338 | 343 | PF00017 | 0.318 |
LIG_WRC_WIRS_1 | 446 | 451 | PF05994 | 0.503 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.562 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.532 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.680 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.591 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.283 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.424 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.682 |
MOD_CK1_1 | 481 | 487 | PF00069 | 0.695 |
MOD_CK1_1 | 501 | 507 | PF00069 | 0.400 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.424 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.436 |
MOD_CK2_1 | 568 | 574 | PF00069 | 0.694 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.428 |
MOD_GlcNHglycan | 165 | 169 | PF01048 | 0.347 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.272 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.368 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.630 |
MOD_GlcNHglycan | 479 | 483 | PF01048 | 0.667 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.532 |
MOD_GlcNHglycan | 497 | 501 | PF01048 | 0.468 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.694 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.614 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.495 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.474 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.461 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.592 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.621 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.740 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.642 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.749 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.518 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.317 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.433 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.601 |
MOD_NEK2_1 | 593 | 598 | PF00069 | 0.607 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.444 |
MOD_PIKK_1 | 294 | 300 | PF00454 | 0.679 |
MOD_PIKK_1 | 35 | 41 | PF00454 | 0.505 |
MOD_PIKK_1 | 532 | 538 | PF00454 | 0.605 |
MOD_PK_1 | 70 | 76 | PF00069 | 0.544 |
MOD_PKA_1 | 174 | 180 | PF00069 | 0.545 |
MOD_PKA_1 | 292 | 298 | PF00069 | 0.531 |
MOD_PKA_1 | 303 | 309 | PF00069 | 0.231 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.545 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.522 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.361 |
MOD_PKA_2 | 521 | 527 | PF00069 | 0.538 |
MOD_PKB_1 | 290 | 298 | PF00069 | 0.700 |
MOD_PKB_1 | 301 | 309 | PF00069 | 0.364 |
MOD_Plk_1 | 423 | 429 | PF00069 | 0.406 |
MOD_Plk_2-3 | 574 | 580 | PF00069 | 0.685 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.333 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.422 |
MOD_Plk_4 | 574 | 580 | PF00069 | 0.734 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.544 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.502 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.313 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.430 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.611 |
MOD_ProDKin_1 | 563 | 569 | PF00069 | 0.668 |
MOD_SUMO_for_1 | 218 | 221 | PF00179 | 0.444 |
MOD_SUMO_rev_2 | 317 | 327 | PF00179 | 0.424 |
TRG_DiLeu_BaLyEn_6 | 48 | 53 | PF01217 | 0.470 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 340 | 343 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 506 | 509 | PF00928 | 0.398 |
TRG_ER_diArg_1 | 290 | 293 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 301 | 304 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 393 | 395 | PF00400 | 0.427 |
TRG_ER_diArg_1 | 428 | 430 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 449 | 452 | PF00400 | 0.523 |
TRG_NES_CRM1_1 | 193 | 206 | PF08389 | 0.532 |
TRG_Pf-PMV_PEXEL_1 | 216 | 221 | PF00026 | 0.244 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMI5 | Leptomonas seymouri | 56% | 99% |
A0A0S4IZ51 | Bodo saltans | 39% | 100% |
A0A1X0P290 | Trypanosomatidae | 45% | 100% |
A0A3S7X363 | Leishmania donovani | 100% | 100% |
A0A422P4X7 | Trypanosoma rangeli | 39% | 100% |
A4HI55 | Leishmania braziliensis | 79% | 100% |
C9ZQR3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9B0M9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q7K3 | Leishmania major | 94% | 100% |
V5BU83 | Trypanosoma cruzi | 41% | 100% |