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: A4HMW7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 284 | 290 | PF00089 | 0.498 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.370 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.518 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 270 | 272 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.518 |
CLV_PCSK_PC1ET2_1 | 26 | 28 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.443 |
CLV_Separin_Metazoa | 293 | 297 | PF03568 | 0.595 |
DEG_APCC_KENBOX_2 | 101 | 105 | PF00400 | 0.721 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.428 |
DEG_SPOP_SBC_1 | 173 | 177 | PF00917 | 0.754 |
DEG_SPOP_SBC_1 | 400 | 404 | PF00917 | 0.706 |
DOC_CYCLIN_RxL_1 | 401 | 414 | PF00134 | 0.638 |
DOC_MAPK_gen_1 | 343 | 352 | PF00069 | 0.604 |
DOC_MAPK_RevD_3 | 11 | 26 | PF00069 | 0.369 |
DOC_PP2B_LxvP_1 | 11 | 14 | PF13499 | 0.369 |
DOC_PP2B_PxIxI_1 | 412 | 418 | PF00149 | 0.617 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.604 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.623 |
LIG_14-3-3_CanoR_1 | 128 | 134 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 225 | 231 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 296 | 304 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 401 | 409 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 83 | 87 | PF00244 | 0.647 |
LIG_APCC_ABBA_1 | 393 | 398 | PF00400 | 0.533 |
LIG_BRCT_BRCA1_1 | 168 | 172 | PF00533 | 0.605 |
LIG_CtBP_PxDLS_1 | 96 | 102 | PF00389 | 0.744 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.539 |
LIG_deltaCOP1_diTrp_1 | 323 | 326 | PF00928 | 0.540 |
LIG_deltaCOP1_diTrp_1 | 414 | 418 | PF00928 | 0.665 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.358 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.587 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.609 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.730 |
LIG_FHA_2 | 141 | 147 | PF00498 | 0.576 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.696 |
LIG_FHA_2 | 298 | 304 | PF00498 | 0.568 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.718 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.643 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.700 |
LIG_LIR_Gen_1 | 263 | 269 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 6 | 16 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 180 | 184 | PF02991 | 0.653 |
LIG_LIR_Nem_3 | 229 | 233 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 263 | 267 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 368 | 372 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 53 | 58 | PF02991 | 0.727 |
LIG_LIR_Nem_3 | 6 | 11 | PF02991 | 0.344 |
LIG_REV1ctd_RIR_1 | 52 | 59 | PF16727 | 0.691 |
LIG_SH2_CRK | 250 | 254 | PF00017 | 0.631 |
LIG_SH2_CRK | 8 | 12 | PF00017 | 0.444 |
LIG_SH2_PTP2 | 264 | 267 | PF00017 | 0.522 |
LIG_SH2_STAP1 | 8 | 12 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.619 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.706 |
LIG_SH2_STAT5 | 453 | 456 | PF00017 | 0.614 |
LIG_SH2_STAT5 | 8 | 11 | PF00017 | 0.444 |
LIG_SH3_1 | 250 | 256 | PF00018 | 0.641 |
LIG_SH3_1 | 338 | 344 | PF00018 | 0.770 |
LIG_SH3_2 | 341 | 346 | PF14604 | 0.780 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.671 |
LIG_SH3_3 | 250 | 256 | PF00018 | 0.607 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.488 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.770 |
LIG_SUMO_SIM_par_1 | 455 | 460 | PF11976 | 0.691 |
LIG_WRC_WIRS_1 | 424 | 429 | PF05994 | 0.697 |
MOD_CDK_SPxxK_3 | 278 | 285 | PF00069 | 0.584 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.739 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.581 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.572 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.714 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.702 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.444 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.623 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.578 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.739 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.713 |
MOD_GlcNHglycan | 146 | 150 | PF01048 | 0.357 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.454 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.412 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.471 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.525 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.470 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.664 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.706 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.712 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.694 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.668 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.747 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.672 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.755 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.609 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.555 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.588 |
MOD_NEK2_2 | 39 | 44 | PF00069 | 0.656 |
MOD_PK_1 | 420 | 426 | PF00069 | 0.689 |
MOD_PKA_1 | 140 | 146 | PF00069 | 0.634 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.634 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.596 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.644 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.628 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.705 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.589 |
MOD_Plk_2-3 | 428 | 434 | PF00069 | 0.714 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.672 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.577 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.287 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.716 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.627 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.650 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.665 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.533 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.568 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.619 |
TRG_DiLeu_BaEn_1 | 195 | 200 | PF01217 | 0.612 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.522 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.706 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.597 |
TRG_ENDOCYTIC_2 | 8 | 11 | PF00928 | 0.444 |
TRG_ER_diArg_1 | 25 | 28 | PF00400 | 0.629 |
TRG_ER_diArg_1 | 269 | 271 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 284 | 287 | PF00400 | 0.620 |
TRG_ER_diArg_1 | 55 | 57 | PF00400 | 0.705 |
TRG_NES_CRM1_1 | 231 | 242 | PF08389 | 0.617 |
TRG_Pf-PMV_PEXEL_1 | 188 | 192 | PF00026 | 0.402 |
TRG_Pf-PMV_PEXEL_1 | 220 | 224 | PF00026 | 0.417 |
TRG_Pf-PMV_PEXEL_1 | 407 | 412 | PF00026 | 0.480 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3G4 | Leptomonas seymouri | 60% | 95% |
A0A1X0P5E8 | Trypanosomatidae | 48% | 100% |
A0A3S7X9P9 | Leishmania donovani | 82% | 100% |
A4IBI8 | Leishmania infantum | 83% | 100% |
C9ZZ52 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AFC4 | Leishmania major | 83% | 100% |
E9B6H9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
V5DUR9 | Trypanosoma cruzi | 47% | 100% |