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: 3 |
Silverman et al. | no | yes: 3 |
Pissara et al. | no | yes: 3 |
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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9APA2
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 |
GO:0007165 | signal transduction | 2 | 2 |
GO:0035556 | intracellular signal transduction | 3 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
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 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 3 |
GO:0004707 | MAP kinase activity | 5 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 174 | 178 | PF00656 | 0.456 |
CLV_C14_Caspase3-7 | 253 | 257 | PF00656 | 0.557 |
CLV_C14_Caspase3-7 | 268 | 272 | PF00656 | 0.468 |
CLV_C14_Caspase3-7 | 351 | 355 | PF00656 | 0.284 |
CLV_C14_Caspase3-7 | 57 | 61 | PF00656 | 0.454 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.361 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 524 | 526 | PF00082 | 0.572 |
CLV_PCSK_PC1ET2_1 | 18 | 20 | PF00082 | 0.447 |
CLV_PCSK_PC1ET2_1 | 524 | 526 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 442 | 446 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 451 | 455 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 541 | 545 | PF00082 | 0.350 |
CLV_Separin_Metazoa | 468 | 472 | PF03568 | 0.331 |
DEG_APCC_DBOX_1 | 540 | 548 | PF00400 | 0.341 |
DEG_COP1_1 | 520 | 529 | PF00400 | 0.539 |
DEG_ODPH_VHL_1 | 186 | 199 | PF01847 | 0.454 |
DEG_SPOP_SBC_1 | 251 | 255 | PF00917 | 0.556 |
DEG_SPOP_SBC_1 | 457 | 461 | PF00917 | 0.186 |
DOC_CYCLIN_RxL_1 | 398 | 408 | PF00134 | 0.361 |
DOC_CYCLIN_RxL_1 | 98 | 105 | PF00134 | 0.328 |
DOC_MAPK_gen_1 | 18 | 24 | PF00069 | 0.434 |
DOC_MAPK_gen_1 | 314 | 323 | PF00069 | 0.270 |
DOC_PP4_FxxP_1 | 136 | 139 | PF00568 | 0.305 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.332 |
DOC_USP7_UBL2_3 | 450 | 454 | PF12436 | 0.320 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 460 | 465 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.240 |
LIG_Actin_WH2_2 | 157 | 175 | PF00022 | 0.324 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.598 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.531 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.531 |
LIG_BIR_III_4 | 269 | 273 | PF00653 | 0.460 |
LIG_EH_1 | 504 | 508 | PF12763 | 0.278 |
LIG_eIF4E_1 | 89 | 95 | PF01652 | 0.435 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.337 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.532 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.397 |
LIG_FHA_1 | 344 | 350 | PF00498 | 0.500 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.211 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.301 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.322 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.426 |
LIG_FHA_2 | 169 | 175 | PF00498 | 0.333 |
LIG_FHA_2 | 180 | 186 | PF00498 | 0.466 |
LIG_FHA_2 | 251 | 257 | PF00498 | 0.651 |
LIG_FHA_2 | 349 | 355 | PF00498 | 0.299 |
LIG_FHA_2 | 463 | 469 | PF00498 | 0.331 |
LIG_FHA_2 | 574 | 580 | PF00498 | 0.396 |
LIG_LIR_Apic_2 | 134 | 139 | PF02991 | 0.317 |
LIG_LIR_Apic_2 | 357 | 363 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 147 | 154 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 159 | 170 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 33 | 43 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 557 | 564 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 134 | 140 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 147 | 151 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 157 | 161 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 288 | 294 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 33 | 38 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 380 | 385 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 39 | 44 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 417 | 422 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 51 | 55 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 511 | 516 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 557 | 562 | PF02991 | 0.497 |
LIG_NRBOX | 33 | 39 | PF00104 | 0.374 |
LIG_NRBOX | 465 | 471 | PF00104 | 0.247 |
LIG_PTB_Apo_2 | 502 | 509 | PF02174 | 0.313 |
LIG_REV1ctd_RIR_1 | 505 | 514 | PF16727 | 0.409 |
LIG_SH2_CRK | 148 | 152 | PF00017 | 0.434 |
LIG_SH2_CRK | 513 | 517 | PF00017 | 0.469 |
LIG_SH2_CRK | 52 | 56 | PF00017 | 0.375 |
LIG_SH2_NCK_1 | 360 | 364 | PF00017 | 0.270 |
LIG_SH2_NCK_1 | 41 | 45 | PF00017 | 0.431 |
LIG_SH2_NCK_1 | 75 | 79 | PF00017 | 0.447 |
LIG_SH2_SRC | 513 | 516 | PF00017 | 0.427 |
LIG_SH2_SRC | 75 | 78 | PF00017 | 0.483 |
LIG_SH2_STAP1 | 148 | 152 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 190 | 194 | PF00017 | 0.524 |
LIG_SH2_STAP1 | 405 | 409 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.360 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.571 |
LIG_SH3_3 | 513 | 519 | PF00018 | 0.443 |
LIG_SUMO_SIM_anti_2 | 476 | 487 | PF11976 | 0.186 |
LIG_SUMO_SIM_par_1 | 280 | 286 | PF11976 | 0.494 |
LIG_SUMO_SIM_par_1 | 364 | 372 | PF11976 | 0.311 |
LIG_TRAF2_1 | 71 | 74 | PF00917 | 0.441 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.614 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.186 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.361 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.186 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.330 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.461 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.460 |
MOD_CK2_1 | 429 | 435 | PF00069 | 0.366 |
MOD_CK2_1 | 462 | 468 | PF00069 | 0.331 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.325 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.425 |
MOD_GlcNHglycan | 424 | 428 | PF01048 | 0.360 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.497 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.402 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.430 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.563 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.288 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.230 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.319 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.506 |
MOD_GSK3_1 | 573 | 580 | PF00069 | 0.461 |
MOD_N-GLC_1 | 342 | 347 | PF02516 | 0.370 |
MOD_N-GLC_1 | 354 | 359 | PF02516 | 0.207 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.322 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.398 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.375 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.380 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.361 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.340 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.343 |
MOD_NEK2_1 | 558 | 563 | PF00069 | 0.410 |
MOD_PIKK_1 | 354 | 360 | PF00454 | 0.288 |
MOD_PIKK_1 | 410 | 416 | PF00454 | 0.278 |
MOD_PK_1 | 525 | 531 | PF00069 | 0.567 |
MOD_PKA_2 | 329 | 335 | PF00069 | 0.394 |
MOD_PKA_2 | 495 | 501 | PF00069 | 0.312 |
MOD_Plk_1 | 168 | 174 | PF00069 | 0.330 |
MOD_Plk_1 | 176 | 182 | PF00069 | 0.411 |
MOD_Plk_1 | 28 | 34 | PF00069 | 0.430 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.361 |
MOD_Plk_1 | 354 | 360 | PF00069 | 0.278 |
MOD_Plk_1 | 480 | 486 | PF00069 | 0.186 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.542 |
MOD_Plk_2-3 | 144 | 150 | PF00069 | 0.397 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.611 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.270 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.332 |
MOD_Plk_4 | 480 | 486 | PF00069 | 0.343 |
MOD_Plk_4 | 558 | 564 | PF00069 | 0.504 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.554 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.368 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.571 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.385 |
MOD_ProDKin_1 | 460 | 466 | PF00069 | 0.335 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.240 |
MOD_SUMO_for_1 | 316 | 319 | PF00179 | 0.301 |
MOD_SUMO_for_1 | 564 | 567 | PF00179 | 0.432 |
MOD_SUMO_rev_2 | 550 | 558 | PF00179 | 0.563 |
MOD_SUMO_rev_2 | 567 | 576 | PF00179 | 0.437 |
TRG_DiLeu_BaEn_1 | 33 | 38 | PF01217 | 0.423 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 297 | 300 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 513 | 516 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 52 | 55 | PF00928 | 0.384 |
TRG_ER_diArg_1 | 194 | 196 | PF00400 | 0.500 |
TRG_Pf-PMV_PEXEL_1 | 101 | 105 | PF00026 | 0.362 |
TRG_Pf-PMV_PEXEL_1 | 314 | 319 | PF00026 | 0.361 |
TRG_Pf-PMV_PEXEL_1 | 420 | 424 | PF00026 | 0.399 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZJ0 | Leptomonas seymouri | 73% | 100% |
A0A3Q8I9M4 | Leishmania donovani | 88% | 95% |
A0A3S5IR55 | Trypanosoma rangeli | 51% | 100% |
A4H641 | Leishmania braziliensis | 30% | 100% |
A4H767 | Leishmania braziliensis | 78% | 100% |
A4HVK6 | Leishmania infantum | 88% | 81% |
Q4QG76 | Leishmania major | 89% | 98% |
Q4QHG6 | Leishmania major | 30% | 100% |
V5AVM7 | Trypanosoma cruzi | 48% | 100% |