Possesses a conserved Fe2+ binding catalytic pocket. Might be involved in some unknown metabolic pathway.. Most similar to Chlamydomonas proteins A0A2K3DQH2 and A0A835WMM9.
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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: E9AFC4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 46 | 50 | PF00656 | 0.713 |
CLV_MEL_PAP_1 | 284 | 290 | PF00089 | 0.527 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.478 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 270 | 272 | PF00082 | 0.369 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.478 |
CLV_PCSK_PC1ET2_1 | 26 | 28 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.432 |
CLV_Separin_Metazoa | 293 | 297 | PF03568 | 0.592 |
DEG_APCC_DBOX_1 | 208 | 216 | PF00400 | 0.606 |
DEG_APCC_DBOX_1 | 450 | 458 | PF00400 | 0.662 |
DEG_APCC_KENBOX_2 | 101 | 105 | PF00400 | 0.686 |
DEG_COP1_1 | 6 | 16 | PF00400 | 0.408 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.416 |
DEG_SPOP_SBC_1 | 173 | 177 | PF00917 | 0.760 |
DEG_SPOP_SBC_1 | 400 | 404 | PF00917 | 0.691 |
DOC_CKS1_1 | 82 | 87 | PF01111 | 0.709 |
DOC_CYCLIN_RxL_1 | 401 | 414 | PF00134 | 0.629 |
DOC_MAPK_MEF2A_6 | 102 | 109 | PF00069 | 0.605 |
DOC_MAPK_RevD_3 | 11 | 26 | PF00069 | 0.369 |
DOC_PP2B_LxvP_1 | 11 | 14 | PF13499 | 0.369 |
DOC_PP2B_LxvP_1 | 370 | 373 | PF13499 | 0.705 |
DOC_PP2B_PxIxI_1 | 13 | 19 | PF00149 | 0.429 |
DOC_PP2B_PxIxI_1 | 412 | 418 | PF00149 | 0.627 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.589 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.746 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 340 | 345 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.729 |
LIG_14-3-3_CanoR_1 | 128 | 134 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 225 | 231 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 285 | 295 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 296 | 300 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 365 | 370 | PF00244 | 0.670 |
LIG_14-3-3_CanoR_1 | 401 | 409 | PF00244 | 0.710 |
LIG_APCC_ABBA_1 | 393 | 398 | PF00400 | 0.528 |
LIG_BIR_III_4 | 438 | 442 | PF00653 | 0.665 |
LIG_CtBP_PxDLS_1 | 115 | 119 | PF00389 | 0.616 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.529 |
LIG_deltaCOP1_diTrp_1 | 224 | 230 | PF00928 | 0.468 |
LIG_deltaCOP1_diTrp_1 | 323 | 326 | PF00928 | 0.535 |
LIG_deltaCOP1_diTrp_1 | 414 | 418 | PF00928 | 0.681 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.358 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.617 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.705 |
LIG_FHA_2 | 298 | 304 | PF00498 | 0.565 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.736 |
LIG_FHA_2 | 44 | 50 | PF00498 | 0.659 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.672 |
LIG_LIR_Gen_1 | 224 | 233 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 263 | 269 | PF02991 | 0.526 |
LIG_LIR_Gen_1 | 6 | 16 | PF02991 | 0.444 |
LIG_LIR_LC3C_4 | 389 | 394 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 180 | 184 | PF02991 | 0.661 |
LIG_LIR_Nem_3 | 224 | 230 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 263 | 267 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 53 | 58 | PF02991 | 0.708 |
LIG_LIR_Nem_3 | 6 | 11 | PF02991 | 0.344 |
LIG_LYPXL_yS_3 | 44 | 47 | PF13949 | 0.642 |
LIG_REV1ctd_RIR_1 | 52 | 59 | PF16727 | 0.674 |
LIG_SH2_CRK | 250 | 254 | PF00017 | 0.641 |
LIG_SH2_CRK | 8 | 12 | PF00017 | 0.444 |
LIG_SH2_PTP2 | 264 | 267 | PF00017 | 0.524 |
LIG_SH2_STAP1 | 8 | 12 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.693 |
LIG_SH2_STAT5 | 453 | 456 | PF00017 | 0.620 |
LIG_SH2_STAT5 | 8 | 11 | PF00017 | 0.444 |
LIG_SH3_1 | 250 | 256 | PF00018 | 0.643 |
LIG_SH3_1 | 338 | 344 | PF00018 | 0.747 |
LIG_SH3_2 | 341 | 346 | PF14604 | 0.761 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.661 |
LIG_SH3_3 | 250 | 256 | PF00018 | 0.608 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.485 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.597 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.747 |
LIG_SH3_3 | 376 | 382 | PF00018 | 0.645 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.698 |
LIG_SUMO_SIM_anti_2 | 303 | 308 | PF11976 | 0.591 |
LIG_SUMO_SIM_par_1 | 455 | 460 | PF11976 | 0.698 |
LIG_UBA3_1 | 358 | 363 | PF00899 | 0.582 |
LIG_WRC_WIRS_1 | 424 | 429 | PF05994 | 0.648 |
MOD_CDC14_SPxK_1 | 343 | 346 | PF00782 | 0.653 |
MOD_CDK_SPxK_1 | 340 | 346 | PF00069 | 0.637 |
MOD_CDK_SPxxK_3 | 278 | 285 | PF00069 | 0.487 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.505 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.563 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.654 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.444 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.716 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.629 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.684 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.565 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.501 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.619 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.650 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.576 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.615 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.686 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.526 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.542 |
MOD_PIKK_1 | 127 | 133 | PF00454 | 0.510 |
MOD_PK_1 | 420 | 426 | PF00069 | 0.633 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.545 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.713 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.592 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.532 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.629 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.565 |
MOD_Plk_1 | 145 | 151 | PF00069 | 0.527 |
MOD_Plk_2-3 | 428 | 434 | PF00069 | 0.687 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.352 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.463 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.340 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.649 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.697 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.398 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.461 |
MOD_ProDKin_1 | 340 | 346 | PF00069 | 0.637 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.673 |
TRG_DiLeu_BaEn_1 | 195 | 200 | PF01217 | 0.543 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.628 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.549 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 8 | 11 | PF00928 | 0.444 |
TRG_ER_diArg_1 | 209 | 212 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 25 | 28 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 269 | 271 | PF00400 | 0.429 |
TRG_ER_diArg_1 | 284 | 287 | PF00400 | 0.573 |
TRG_ER_diArg_1 | 55 | 57 | PF00400 | 0.615 |
TRG_NES_CRM1_1 | 231 | 242 | PF08389 | 0.503 |
TRG_NLS_MonoExtN_4 | 139 | 144 | PF00514 | 0.502 |
TRG_Pf-PMV_PEXEL_1 | 188 | 192 | PF00026 | 0.510 |
TRG_Pf-PMV_PEXEL_1 | 220 | 224 | PF00026 | 0.505 |
TRG_Pf-PMV_PEXEL_1 | 407 | 412 | PF00026 | 0.593 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3G4 | Leptomonas seymouri | 62% | 95% |
A0A1X0P5E8 | Trypanosomatidae | 49% | 100% |
A0A3S7X9P9 | Leishmania donovani | 94% | 100% |
A4HMW7 | Leishmania braziliensis | 83% | 100% |
A4IBI8 | Leishmania infantum | 95% | 100% |
C9ZZ52 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9B6H9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5DUR9 | Trypanosoma cruzi | 47% | 100% |