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: A4HKB7
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 | 139 | 143 | PF00656 | 0.633 |
CLV_C14_Caspase3-7 | 457 | 461 | PF00656 | 0.394 |
CLV_C14_Caspase3-7 | 90 | 94 | PF00656 | 0.530 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.738 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.735 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 536 | 538 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 543 | 545 | PF00675 | 0.477 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 536 | 538 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 543 | 545 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 558 | 560 | PF00082 | 0.589 |
CLV_PCSK_PC7_1 | 554 | 560 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 502 | 506 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 544 | 548 | PF00082 | 0.518 |
CLV_Separin_Metazoa | 104 | 108 | PF03568 | 0.522 |
CLV_Separin_Metazoa | 519 | 523 | PF03568 | 0.531 |
DEG_APCC_DBOX_1 | 174 | 182 | PF00400 | 0.356 |
DEG_SCF_FBW7_1 | 399 | 406 | PF00400 | 0.447 |
DOC_CYCLIN_yCln2_LP_2 | 527 | 533 | PF00134 | 0.290 |
DOC_MAPK_gen_1 | 214 | 222 | PF00069 | 0.313 |
DOC_MAPK_MEF2A_6 | 266 | 274 | PF00069 | 0.494 |
DOC_PP2B_LxvP_1 | 256 | 259 | PF13499 | 0.379 |
DOC_PP2B_LxvP_1 | 272 | 275 | PF13499 | 0.382 |
DOC_PP4_FxxP_1 | 243 | 246 | PF00568 | 0.657 |
DOC_PP4_FxxP_1 | 80 | 83 | PF00568 | 0.761 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.426 |
DOC_USP7_UBL2_3 | 206 | 210 | PF12436 | 0.537 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.359 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 467 | 472 | PF00397 | 0.427 |
LIG_14-3-3_CanoR_1 | 130 | 136 | PF00244 | 0.728 |
LIG_14-3-3_CanoR_1 | 332 | 340 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 522 | 527 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 543 | 547 | PF00244 | 0.284 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.752 |
LIG_BRCT_BRCA1_1 | 239 | 243 | PF00533 | 0.720 |
LIG_CSL_BTD_1 | 192 | 195 | PF09270 | 0.446 |
LIG_deltaCOP1_diTrp_1 | 431 | 435 | PF00928 | 0.447 |
LIG_deltaCOP1_diTrp_1 | 548 | 555 | PF00928 | 0.323 |
LIG_eIF4E_1 | 251 | 257 | PF01652 | 0.502 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.460 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.227 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.406 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.339 |
LIG_FHA_2 | 372 | 378 | PF00498 | 0.355 |
LIG_FHA_2 | 442 | 448 | PF00498 | 0.335 |
LIG_FHA_2 | 543 | 549 | PF00498 | 0.540 |
LIG_Integrin_RGD_1 | 61 | 63 | PF01839 | 0.511 |
LIG_LIR_Apic_2 | 240 | 246 | PF02991 | 0.679 |
LIG_LIR_Gen_1 | 248 | 259 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 395 | 403 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 145 | 151 | PF02991 | 0.642 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 334 | 340 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 395 | 399 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 529 | 535 | PF02991 | 0.443 |
LIG_LYPXL_S_1 | 26 | 30 | PF13949 | 0.531 |
LIG_LYPXL_yS_3 | 27 | 30 | PF13949 | 0.531 |
LIG_MYND_1 | 242 | 246 | PF01753 | 0.669 |
LIG_NRP_CendR_1 | 558 | 560 | PF00754 | 0.447 |
LIG_REV1ctd_RIR_1 | 78 | 82 | PF16727 | 0.519 |
LIG_SH2_CRK | 251 | 255 | PF00017 | 0.510 |
LIG_SH2_STAP1 | 314 | 318 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.718 |
LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.451 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.552 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.622 |
LIG_TRAF2_1 | 245 | 248 | PF00917 | 0.579 |
LIG_UBA3_1 | 504 | 510 | PF00899 | 0.378 |
MOD_CDK_SPxK_1 | 401 | 407 | PF00069 | 0.480 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.520 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.721 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.628 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.564 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.502 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.372 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.507 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.449 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.755 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.447 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.362 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.333 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.755 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.784 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.507 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.461 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.606 |
MOD_CK2_1 | 277 | 283 | PF00069 | 0.488 |
MOD_CK2_1 | 522 | 528 | PF00069 | 0.493 |
MOD_CK2_1 | 542 | 548 | PF00069 | 0.208 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.504 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.738 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.749 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.498 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.493 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.227 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.748 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.675 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.726 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.603 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.513 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.631 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.674 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.674 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.447 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.725 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.388 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.442 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.443 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.741 |
MOD_N-GLC_1 | 131 | 136 | PF02516 | 0.741 |
MOD_N-GLC_1 | 277 | 282 | PF02516 | 0.504 |
MOD_N-GLC_1 | 308 | 313 | PF02516 | 0.653 |
MOD_N-GLC_1 | 32 | 37 | PF02516 | 0.549 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.544 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.507 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.441 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.514 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.750 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.535 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.406 |
MOD_NEK2_2 | 277 | 282 | PF00069 | 0.499 |
MOD_NEK2_2 | 542 | 547 | PF00069 | 0.481 |
MOD_NEK2_2 | 56 | 61 | PF00069 | 0.522 |
MOD_PIKK_1 | 487 | 493 | PF00454 | 0.317 |
MOD_PKA_1 | 107 | 113 | PF00069 | 0.738 |
MOD_PKA_1 | 130 | 136 | PF00069 | 0.728 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.661 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.433 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.391 |
MOD_PKA_2 | 230 | 236 | PF00069 | 0.665 |
MOD_PKA_2 | 331 | 337 | PF00069 | 0.527 |
MOD_PKA_2 | 542 | 548 | PF00069 | 0.285 |
MOD_PKB_1 | 129 | 137 | PF00069 | 0.550 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.631 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.445 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.494 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.421 |
MOD_Plk_1 | 318 | 324 | PF00069 | 0.567 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.525 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.778 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.433 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.513 |
MOD_Plk_4 | 289 | 295 | PF00069 | 0.446 |
MOD_Plk_4 | 522 | 528 | PF00069 | 0.537 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.650 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.534 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.550 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.668 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.359 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.335 |
MOD_ProDKin_1 | 467 | 473 | PF00069 | 0.417 |
MOD_SUMO_rev_2 | 13 | 21 | PF00179 | 0.486 |
TRG_DiLeu_BaEn_1 | 268 | 273 | PF01217 | 0.530 |
TRG_DiLeu_BaEn_1 | 500 | 505 | PF01217 | 0.509 |
TRG_DiLeu_BaEn_2 | 354 | 360 | PF01217 | 0.480 |
TRG_DiLeu_BaEn_2 | 527 | 533 | PF01217 | 0.543 |
TRG_DiLeu_BaEn_4 | 528 | 534 | PF01217 | 0.510 |
TRG_DiLeu_BaLyEn_6 | 177 | 182 | PF01217 | 0.393 |
TRG_DiLeu_BaLyEn_6 | 459 | 464 | PF01217 | 0.578 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.689 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.451 |
TRG_ER_diArg_1 | 129 | 131 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 411 | 413 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 535 | 537 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 558 | 560 | PF00400 | 0.559 |
TRG_Pf-PMV_PEXEL_1 | 502 | 506 | PF00026 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 82 | 86 | PF00026 | 0.774 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEH1 | Leptomonas seymouri | 66% | 100% |
A0A1X0NUL0 | Trypanosomatidae | 38% | 100% |
A0A3S7X5E9 | Leishmania donovani | 73% | 99% |
A0A422P1A6 | Trypanosoma rangeli | 39% | 100% |
A4I7U6 | Leishmania infantum | 72% | 100% |
D0AA04 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9B2Q4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 99% |
Q4Q5F3 | Leishmania major | 71% | 100% |
V5BGP5 | Trypanosoma cruzi | 39% | 100% |