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: E9B2Q4
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 | 327 | 331 | PF00656 | 0.658 |
CLV_C14_Caspase3-7 | 469 | 473 | PF00656 | 0.586 |
CLV_C14_Caspase3-7 | 47 | 51 | PF00656 | 0.681 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 424 | 426 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 548 | 550 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 566 | 568 | PF00675 | 0.433 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 508 | 510 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 548 | 550 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.384 |
CLV_PCSK_PC1ET2_1 | 508 | 510 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.370 |
CLV_Separin_Metazoa | 531 | 535 | PF03568 | 0.519 |
DEG_SCF_FBW7_1 | 411 | 418 | PF00400 | 0.447 |
DEG_SPOP_SBC_1 | 140 | 144 | PF00917 | 0.704 |
DEG_SPOP_SBC_1 | 308 | 312 | PF00917 | 0.460 |
DEG_SPOP_SBC_1 | 329 | 333 | PF00917 | 0.659 |
DEG_SPOP_SBC_1 | 338 | 342 | PF00917 | 0.463 |
DOC_CKS1_1 | 254 | 259 | PF01111 | 0.540 |
DOC_MAPK_MEF2A_6 | 261 | 269 | PF00069 | 0.360 |
DOC_MAPK_MEF2A_6 | 493 | 500 | PF00069 | 0.525 |
DOC_PP1_RVXF_1 | 482 | 489 | PF00149 | 0.588 |
DOC_PP2B_LxvP_1 | 267 | 270 | PF13499 | 0.376 |
DOC_PP2B_LxvP_1 | 283 | 286 | PF13499 | 0.368 |
DOC_PP4_FxxP_1 | 254 | 257 | PF00568 | 0.631 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.426 |
DOC_USP7_UBL2_3 | 213 | 217 | PF12436 | 0.564 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.359 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.335 |
LIG_14-3-3_CanoR_1 | 102 | 112 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 189 | 197 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 344 | 350 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 40 | 45 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 534 | 539 | PF00244 | 0.482 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.739 |
LIG_BRCT_BRCA1_1 | 2 | 6 | PF00533 | 0.667 |
LIG_BRCT_BRCA1_1 | 250 | 254 | PF00533 | 0.705 |
LIG_BRCT_BRCA1_1 | 339 | 343 | PF00533 | 0.582 |
LIG_BRCT_BRCA1_1 | 40 | 44 | PF00533 | 0.568 |
LIG_CaM_IQ_9 | 514 | 529 | PF13499 | 0.246 |
LIG_CtBP_PxDLS_1 | 313 | 317 | PF00389 | 0.464 |
LIG_deltaCOP1_diTrp_1 | 443 | 447 | PF00928 | 0.447 |
LIG_eIF4E_1 | 262 | 268 | PF01652 | 0.492 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.678 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.406 |
LIG_FHA_1 | 481 | 487 | PF00498 | 0.576 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.476 |
LIG_FHA_2 | 104 | 110 | PF00498 | 0.422 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.544 |
LIG_FHA_2 | 384 | 390 | PF00498 | 0.355 |
LIG_FHA_2 | 454 | 460 | PF00498 | 0.335 |
LIG_FHA_2 | 555 | 561 | PF00498 | 0.530 |
LIG_LIR_Apic_2 | 251 | 257 | PF02991 | 0.664 |
LIG_LIR_Gen_1 | 121 | 130 | PF02991 | 0.753 |
LIG_LIR_Gen_1 | 259 | 270 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 407 | 415 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 121 | 125 | PF02991 | 0.751 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.624 |
LIG_LIR_Nem_3 | 259 | 265 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 346 | 352 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 407 | 411 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 541 | 547 | PF02991 | 0.432 |
LIG_LYPXL_S_1 | 26 | 30 | PF13949 | 0.536 |
LIG_LYPXL_yS_3 | 27 | 30 | PF13949 | 0.533 |
LIG_MYND_1 | 253 | 257 | PF01753 | 0.643 |
LIG_PCNA_yPIPBox_3 | 102 | 112 | PF02747 | 0.423 |
LIG_SH2_CRK | 262 | 266 | PF00017 | 0.497 |
LIG_SH2_NCK_1 | 70 | 74 | PF00017 | 0.565 |
LIG_SH2_PTP2 | 25 | 28 | PF00017 | 0.459 |
LIG_SH2_SRC | 25 | 28 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.723 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 70 | 73 | PF00017 | 0.569 |
LIG_SH3_3 | 179 | 185 | PF00018 | 0.510 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.677 |
LIG_SUMO_SIM_anti_2 | 497 | 502 | PF11976 | 0.469 |
LIG_SUMO_SIM_par_1 | 310 | 317 | PF11976 | 0.666 |
LIG_SUMO_SIM_par_1 | 450 | 456 | PF11976 | 0.338 |
LIG_TRAF2_1 | 256 | 259 | PF00917 | 0.560 |
LIG_UBA3_1 | 516 | 522 | PF00899 | 0.370 |
MOD_CDK_SPxK_1 | 413 | 419 | PF00069 | 0.480 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.733 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.703 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.604 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.483 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.559 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.443 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.449 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.724 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.447 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.341 |
MOD_CK1_1 | 552 | 558 | PF00069 | 0.445 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.750 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.450 |
MOD_CK2_1 | 120 | 126 | PF00069 | 0.771 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.450 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.578 |
MOD_CK2_1 | 288 | 294 | PF00069 | 0.477 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.475 |
MOD_CK2_1 | 554 | 560 | PF00069 | 0.197 |
MOD_Cter_Amidation | 506 | 509 | PF01082 | 0.456 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.702 |
MOD_GlcNHglycan | 121 | 125 | PF01048 | 0.680 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.656 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.736 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.538 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.493 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.713 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.683 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.710 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.627 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.542 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.500 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.601 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.492 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.680 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.517 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.447 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.388 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.442 |
MOD_N-GLC_1 | 132 | 137 | PF02516 | 0.767 |
MOD_N-GLC_1 | 288 | 293 | PF02516 | 0.489 |
MOD_N-GLC_1 | 48 | 53 | PF02516 | 0.581 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.643 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.583 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.494 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.733 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.500 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.406 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.466 |
MOD_NEK2_2 | 288 | 293 | PF00069 | 0.484 |
MOD_NEK2_2 | 554 | 559 | PF00069 | 0.469 |
MOD_PIKK_1 | 189 | 195 | PF00454 | 0.480 |
MOD_PIKK_1 | 241 | 247 | PF00454 | 0.375 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.422 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.534 |
MOD_PKA_2 | 480 | 486 | PF00069 | 0.613 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.663 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.729 |
MOD_Plk_1 | 120 | 126 | PF00069 | 0.620 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.658 |
MOD_Plk_1 | 226 | 232 | PF00069 | 0.483 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.410 |
MOD_Plk_1 | 549 | 555 | PF00069 | 0.459 |
MOD_Plk_2-3 | 93 | 99 | PF00069 | 0.575 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.422 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.502 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.327 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.519 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.693 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.596 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.625 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.646 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.359 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.335 |
MOD_SUMO_rev_2 | 205 | 215 | PF00179 | 0.584 |
TRG_DiLeu_BaEn_1 | 279 | 284 | PF01217 | 0.529 |
TRG_DiLeu_BaEn_1 | 512 | 517 | PF01217 | 0.496 |
TRG_DiLeu_BaEn_2 | 366 | 372 | PF01217 | 0.480 |
TRG_DiLeu_BaEn_2 | 539 | 545 | PF01217 | 0.531 |
TRG_DiLeu_BaEn_4 | 540 | 546 | PF01217 | 0.499 |
TRG_DiLeu_BaLyEn_6 | 471 | 476 | PF01217 | 0.561 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.689 |
TRG_ENDOCYTIC_2 | 262 | 265 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.691 |
TRG_ENDOCYTIC_2 | 349 | 352 | PF00928 | 0.457 |
TRG_ER_diArg_1 | 423 | 425 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 547 | 549 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 566 | 568 | PF00400 | 0.319 |
TRG_Pf-PMV_PEXEL_1 | 484 | 489 | PF00026 | 0.562 |
TRG_Pf-PMV_PEXEL_1 | 508 | 512 | PF00026 | 0.459 |
TRG_Pf-PMV_PEXEL_1 | 82 | 86 | PF00026 | 0.778 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEH1 | Leptomonas seymouri | 65% | 100% |
A0A1X0NUL0 | Trypanosomatidae | 39% | 100% |
A0A3S7X5E9 | Leishmania donovani | 88% | 100% |
A0A422P1A6 | Trypanosoma rangeli | 39% | 100% |
A4HKB7 | Leishmania braziliensis | 70% | 99% |
A4I7U6 | Leishmania infantum | 87% | 100% |
D0AA04 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
Q4Q5F3 | Leishmania major | 88% | 99% |
V5BGP5 | Trypanosoma cruzi | 39% | 100% |