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: A4I7U6
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 | 132 | 136 | PF00656 | 0.611 |
CLV_C14_Caspase3-7 | 311 | 315 | PF00656 | 0.669 |
CLV_C14_Caspase3-7 | 453 | 457 | PF00656 | 0.607 |
CLV_C14_Caspase3-7 | 47 | 51 | PF00656 | 0.634 |
CLV_NRD_NRD_1 | 408 | 410 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 485 | 487 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 532 | 534 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 550 | 552 | PF00675 | 0.442 |
CLV_PCSK_FUR_1 | 548 | 552 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 408 | 410 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 485 | 487 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 492 | 494 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 532 | 534 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 550 | 552 | PF00082 | 0.394 |
CLV_PCSK_PC1ET2_1 | 492 | 494 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 540 | 544 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.557 |
CLV_Separin_Metazoa | 515 | 519 | PF03568 | 0.528 |
DEG_SCF_FBW7_1 | 395 | 402 | PF00400 | 0.447 |
DEG_SPOP_SBC_1 | 127 | 131 | PF00917 | 0.679 |
DEG_SPOP_SBC_1 | 313 | 317 | PF00917 | 0.665 |
DEG_SPOP_SBC_1 | 322 | 326 | PF00917 | 0.498 |
DOC_CKS1_1 | 238 | 243 | PF01111 | 0.540 |
DOC_CYCLIN_yCln2_LP_2 | 63 | 66 | PF00134 | 0.616 |
DOC_MAPK_gen_1 | 261 | 271 | PF00069 | 0.399 |
DOC_MAPK_MEF2A_6 | 261 | 269 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 477 | 484 | PF00069 | 0.537 |
DOC_PP1_RVXF_1 | 466 | 473 | PF00149 | 0.585 |
DOC_PP2B_LxvP_1 | 251 | 254 | PF13499 | 0.375 |
DOC_PP2B_LxvP_1 | 267 | 270 | PF13499 | 0.366 |
DOC_PP2B_LxvP_1 | 63 | 66 | PF13499 | 0.616 |
DOC_PP4_FxxP_1 | 238 | 241 | PF00568 | 0.631 |
DOC_PP4_FxxP_1 | 67 | 70 | PF00568 | 0.746 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.426 |
DOC_USP7_UBL2_3 | 200 | 204 | PF12436 | 0.539 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.359 |
DOC_WW_Pin1_4 | 414 | 419 | PF00397 | 0.335 |
LIG_14-3-3_CanoR_1 | 195 | 203 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 230 | 239 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 328 | 334 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 518 | 523 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 81 | 89 | PF00244 | 0.599 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.725 |
LIG_BRCT_BRCA1_1 | 2 | 6 | PF00533 | 0.645 |
LIG_BRCT_BRCA1_1 | 234 | 238 | PF00533 | 0.691 |
LIG_BRCT_BRCA1_1 | 323 | 327 | PF00533 | 0.616 |
LIG_deltaCOP1_diTrp_1 | 427 | 431 | PF00928 | 0.447 |
LIG_eIF4E_1 | 246 | 252 | PF01652 | 0.491 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.406 |
LIG_FHA_1 | 465 | 471 | PF00498 | 0.573 |
LIG_FHA_1 | 537 | 543 | PF00498 | 0.482 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.518 |
LIG_FHA_2 | 130 | 136 | PF00498 | 0.653 |
LIG_FHA_2 | 187 | 193 | PF00498 | 0.669 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.545 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.355 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.335 |
LIG_FHA_2 | 539 | 545 | PF00498 | 0.535 |
LIG_LIR_Apic_2 | 235 | 241 | PF02991 | 0.654 |
LIG_LIR_Gen_1 | 108 | 117 | PF02991 | 0.721 |
LIG_LIR_Gen_1 | 243 | 254 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 391 | 399 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 108 | 112 | PF02991 | 0.728 |
LIG_LIR_Nem_3 | 138 | 144 | PF02991 | 0.620 |
LIG_LIR_Nem_3 | 243 | 249 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 330 | 336 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 391 | 395 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 525 | 531 | PF02991 | 0.435 |
LIG_MYND_1 | 237 | 241 | PF01753 | 0.644 |
LIG_PCNA_TLS_4 | 92 | 99 | PF02747 | 0.475 |
LIG_RPA_C_Fungi | 481 | 493 | PF08784 | 0.450 |
LIG_SH2_CRK | 246 | 250 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.706 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.451 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.517 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.655 |
LIG_SUMO_SIM_par_1 | 434 | 440 | PF11976 | 0.338 |
LIG_TRAF2_1 | 240 | 243 | PF00917 | 0.557 |
LIG_UBA3_1 | 500 | 506 | PF00899 | 0.383 |
MOD_CDK_SPxK_1 | 397 | 403 | PF00069 | 0.480 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.709 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.642 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.617 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.496 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.345 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.403 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.449 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.447 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.684 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.341 |
MOD_CK1_1 | 536 | 542 | PF00069 | 0.449 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.518 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.731 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.747 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.571 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.450 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.579 |
MOD_CK2_1 | 272 | 278 | PF00069 | 0.474 |
MOD_CK2_1 | 518 | 524 | PF00069 | 0.485 |
MOD_CK2_1 | 538 | 544 | PF00069 | 0.202 |
MOD_Cter_Amidation | 490 | 493 | PF01082 | 0.479 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.692 |
MOD_GlcNHglycan | 108 | 112 | PF01048 | 0.657 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.716 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.493 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.656 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.682 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.604 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.508 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.606 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.677 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.559 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.447 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.388 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.442 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.706 |
MOD_N-GLC_1 | 119 | 124 | PF02516 | 0.736 |
MOD_N-GLC_1 | 272 | 277 | PF02516 | 0.487 |
MOD_N-GLC_2 | 119 | 121 | PF02516 | 0.703 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.560 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.507 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.735 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.524 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.406 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.466 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.627 |
MOD_NEK2_2 | 272 | 277 | PF00069 | 0.483 |
MOD_NEK2_2 | 538 | 543 | PF00069 | 0.476 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.417 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.565 |
MOD_PKA_2 | 327 | 333 | PF00069 | 0.558 |
MOD_PKA_2 | 464 | 470 | PF00069 | 0.605 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.718 |
MOD_PKB_1 | 228 | 236 | PF00069 | 0.562 |
MOD_Plk_1 | 107 | 113 | PF00069 | 0.595 |
MOD_Plk_1 | 119 | 125 | PF00069 | 0.629 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.489 |
MOD_Plk_1 | 272 | 278 | PF00069 | 0.407 |
MOD_Plk_1 | 533 | 539 | PF00069 | 0.463 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.417 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.656 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.508 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.327 |
MOD_Plk_4 | 518 | 524 | PF00069 | 0.529 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.664 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.641 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.609 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.359 |
MOD_ProDKin_1 | 414 | 420 | PF00069 | 0.335 |
MOD_SUMO_rev_2 | 192 | 202 | PF00179 | 0.564 |
TRG_DiLeu_BaEn_1 | 263 | 268 | PF01217 | 0.526 |
TRG_DiLeu_BaEn_1 | 496 | 501 | PF01217 | 0.512 |
TRG_DiLeu_BaEn_2 | 350 | 356 | PF01217 | 0.480 |
TRG_DiLeu_BaEn_2 | 523 | 529 | PF01217 | 0.535 |
TRG_DiLeu_BaLyEn_6 | 455 | 460 | PF01217 | 0.598 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.665 |
TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.469 |
TRG_ER_diArg_1 | 407 | 409 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 484 | 486 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 531 | 533 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 548 | 551 | PF00400 | 0.312 |
TRG_Pf-PMV_PEXEL_1 | 468 | 473 | PF00026 | 0.564 |
TRG_Pf-PMV_PEXEL_1 | 492 | 496 | PF00026 | 0.473 |
TRG_Pf-PMV_PEXEL_1 | 498 | 502 | PF00026 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 69 | 73 | PF00026 | 0.765 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEH1 | Leptomonas seymouri | 66% | 100% |
A0A1X0NUL0 | Trypanosomatidae | 38% | 100% |
A0A3S7X5E9 | Leishmania donovani | 97% | 98% |
A0A422P1A6 | Trypanosoma rangeli | 39% | 100% |
A4HKB7 | Leishmania braziliensis | 72% | 99% |
D0AA04 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9B2Q4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4Q5F3 | Leishmania major | 91% | 100% |
V5BGP5 | Trypanosoma cruzi | 40% | 100% |