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:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4IBX2
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 1 |
GO:0006644 | phospholipid metabolic process | 4 | 1 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008610 | lipid biosynthetic process | 4 | 1 |
GO:0008654 | phospholipid biosynthetic process | 5 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019637 | organophosphate metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044255 | cellular lipid metabolic process | 3 | 1 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 1 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 1 |
GO:0046486 | glycerolipid metabolic process | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090407 | organophosphate biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.254 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.404 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.286 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.404 |
CLV_PCSK_PC1ET2_1 | 315 | 317 | PF00082 | 0.543 |
CLV_PCSK_PC1ET2_1 | 426 | 428 | PF00082 | 0.302 |
CLV_PCSK_PC7_1 | 9 | 15 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.575 |
DEG_APCC_DBOX_1 | 392 | 400 | PF00400 | 0.370 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.622 |
DEG_ODPH_VHL_1 | 263 | 275 | PF01847 | 0.445 |
DEG_SPOP_SBC_1 | 171 | 175 | PF00917 | 0.688 |
DOC_CKS1_1 | 365 | 370 | PF01111 | 0.469 |
DOC_CKS1_1 | 500 | 505 | PF01111 | 0.357 |
DOC_CYCLIN_RxL_1 | 512 | 522 | PF00134 | 0.342 |
DOC_CYCLIN_RxL_1 | 6 | 15 | PF00134 | 0.515 |
DOC_CYCLIN_yCln2_LP_2 | 218 | 224 | PF00134 | 0.437 |
DOC_MAPK_gen_1 | 213 | 220 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 213 | 222 | PF00069 | 0.447 |
DOC_PP2B_LxvP_1 | 218 | 221 | PF13499 | 0.437 |
DOC_PP2B_LxvP_1 | 262 | 265 | PF13499 | 0.448 |
DOC_PP2B_LxvP_1 | 350 | 353 | PF13499 | 0.398 |
DOC_PP4_FxxP_1 | 22 | 25 | PF00568 | 0.462 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.433 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 499 | 504 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.668 |
LIG_14-3-3_CanoR_1 | 2 | 7 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 213 | 219 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 290 | 296 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 482 | 486 | PF00244 | 0.439 |
LIG_EH1_1 | 511 | 519 | PF00400 | 0.425 |
LIG_eIF4E_1 | 199 | 205 | PF01652 | 0.480 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.424 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.539 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.504 |
LIG_FHA_2 | 30 | 36 | PF00498 | 0.570 |
LIG_FHA_2 | 343 | 349 | PF00498 | 0.369 |
LIG_LIR_Apic_2 | 162 | 167 | PF02991 | 0.576 |
LIG_LIR_Apic_2 | 502 | 508 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 337 | 347 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 398 | 408 | PF02991 | 0.387 |
LIG_LIR_LC3C_4 | 270 | 275 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 321 | 327 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 337 | 343 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 398 | 403 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 5 | 11 | PF02991 | 0.600 |
LIG_LYPXL_SIV_4 | 368 | 376 | PF13949 | 0.468 |
LIG_LYPXL_SIV_4 | 420 | 428 | PF13949 | 0.368 |
LIG_NRBOX | 239 | 245 | PF00104 | 0.539 |
LIG_NRBOX | 346 | 352 | PF00104 | 0.365 |
LIG_Pex14_2 | 22 | 26 | PF04695 | 0.466 |
LIG_Pex14_2 | 442 | 446 | PF04695 | 0.302 |
LIG_SH2_CRK | 413 | 417 | PF00017 | 0.289 |
LIG_SH2_CRK | 8 | 12 | PF00017 | 0.662 |
LIG_SH2_NCK_1 | 400 | 404 | PF00017 | 0.507 |
LIG_SH2_PTP2 | 164 | 167 | PF00017 | 0.605 |
LIG_SH2_PTP2 | 505 | 508 | PF00017 | 0.351 |
LIG_SH2_SRC | 164 | 167 | PF00017 | 0.581 |
LIG_SH2_STAP1 | 117 | 121 | PF00017 | 0.387 |
LIG_SH2_STAP1 | 161 | 165 | PF00017 | 0.548 |
LIG_SH2_STAP1 | 490 | 494 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 18 | 21 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 505 | 508 | PF00017 | 0.351 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.584 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.462 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.386 |
LIG_SH3_3 | 497 | 503 | PF00018 | 0.374 |
LIG_SUMO_SIM_anti_2 | 269 | 276 | PF11976 | 0.542 |
LIG_SUMO_SIM_anti_2 | 345 | 351 | PF11976 | 0.369 |
LIG_SUMO_SIM_par_1 | 190 | 195 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 483 | 489 | PF11976 | 0.462 |
LIG_TRAF2_1 | 32 | 35 | PF00917 | 0.594 |
LIG_TRAF2_1 | 71 | 74 | PF00917 | 0.515 |
MOD_CDC14_SPxK_1 | 258 | 261 | PF00782 | 0.539 |
MOD_CDK_SPxK_1 | 255 | 261 | PF00069 | 0.504 |
MOD_CDK_SPxK_1 | 98 | 104 | PF00069 | 0.665 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.710 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.655 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.698 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.733 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.492 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.474 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.490 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.515 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.643 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.696 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.318 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.272 |
MOD_GlcNHglycan | 238 | 243 | PF01048 | 0.230 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.494 |
MOD_GlcNHglycan | 430 | 434 | PF01048 | 0.370 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.274 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.649 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.652 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.697 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.590 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.406 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.496 |
MOD_N-GLC_1 | 125 | 130 | PF02516 | 0.706 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.609 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.523 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.662 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.326 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.428 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.445 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.561 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.368 |
MOD_NEK2_1 | 525 | 530 | PF00069 | 0.599 |
MOD_PIKK_1 | 128 | 134 | PF00454 | 0.571 |
MOD_PK_1 | 291 | 297 | PF00069 | 0.391 |
MOD_PK_1 | 483 | 489 | PF00069 | 0.588 |
MOD_PKA_1 | 213 | 219 | PF00069 | 0.527 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.573 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.461 |
MOD_PKB_1 | 427 | 435 | PF00069 | 0.217 |
MOD_Plk_1 | 137 | 143 | PF00069 | 0.682 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.480 |
MOD_Plk_2-3 | 342 | 348 | PF00069 | 0.384 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.623 |
MOD_Plk_4 | 342 | 348 | PF00069 | 0.377 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.490 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.678 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.612 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.500 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.697 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.442 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.438 |
MOD_ProDKin_1 | 499 | 505 | PF00069 | 0.415 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.491 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.665 |
MOD_SUMO_rev_2 | 151 | 158 | PF00179 | 0.615 |
MOD_SUMO_rev_2 | 27 | 33 | PF00179 | 0.461 |
TRG_DiLeu_BaEn_1 | 239 | 244 | PF01217 | 0.462 |
TRG_DiLeu_BaEn_1 | 269 | 274 | PF01217 | 0.491 |
TRG_DiLeu_BaEn_3 | 90 | 96 | PF01217 | 0.593 |
TRG_DiLeu_BaEn_4 | 73 | 79 | PF01217 | 0.593 |
TRG_DiLeu_BaLyEn_6 | 200 | 205 | PF01217 | 0.569 |
TRG_DiLeu_BaLyEn_6 | 258 | 263 | PF01217 | 0.539 |
TRG_ENDOCYTIC_2 | 400 | 403 | PF00928 | 0.511 |
TRG_ENDOCYTIC_2 | 8 | 11 | PF00928 | 0.662 |
TRG_ER_diArg_1 | 12 | 14 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 20 | 22 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 289 | 291 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 76 | 78 | PF00400 | 0.549 |
TRG_Pf-PMV_PEXEL_1 | 261 | 266 | PF00026 | 0.339 |
TRG_Pf-PMV_PEXEL_1 | 426 | 430 | PF00026 | 0.302 |
TRG_Pf-PMV_PEXEL_1 | 483 | 488 | PF00026 | 0.406 |
TRG_Pf-PMV_PEXEL_1 | 58 | 62 | PF00026 | 0.601 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5I3 | Leptomonas seymouri | 73% | 100% |
A0A0S4JPF8 | Bodo saltans | 54% | 100% |
A0A1X0P5B2 | Trypanosomatidae | 59% | 100% |
A0A3Q8IMX2 | Leishmania donovani | 100% | 100% |
A0A3R7L7A5 | Trypanosoma rangeli | 61% | 100% |
A4HNA1 | Leishmania braziliensis | 84% | 100% |
C9ZYN6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
E9AFQ9 | Leishmania major | 95% | 100% |
E9B6W2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
V5BCR1 | Trypanosoma cruzi | 62% | 100% |