The closest related human enzyme is a retinol dehydrogenase. Anchored to the membrane from the inner side.. Localization: ER (by homology)
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 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: E9AE70
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 441 | 445 | PF00656 | 0.596 |
CLV_MEL_PAP_1 | 7 | 13 | PF00089 | 0.603 |
CLV_NRD_NRD_1 | 372 | 374 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.451 |
CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.352 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.451 |
CLV_PCSK_PC1ET2_1 | 46 | 48 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.466 |
DEG_APCC_DBOX_1 | 22 | 30 | PF00400 | 0.266 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.343 |
DOC_CYCLIN_RxL_1 | 136 | 147 | PF00134 | 0.632 |
DOC_CYCLIN_yCln2_LP_2 | 248 | 251 | PF00134 | 0.594 |
DOC_MAPK_MEF2A_6 | 240 | 248 | PF00069 | 0.628 |
DOC_PP1_RVXF_1 | 8 | 14 | PF00149 | 0.487 |
DOC_PP2B_LxvP_1 | 248 | 251 | PF13499 | 0.594 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.567 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.635 |
LIG_14-3-3_CanoR_1 | 10 | 14 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 207 | 213 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 235 | 244 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 446 | 451 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 68 | 73 | PF00244 | 0.609 |
LIG_Actin_WH2_2 | 179 | 195 | PF00022 | 0.547 |
LIG_Actin_WH2_2 | 339 | 357 | PF00022 | 0.642 |
LIG_APCC_ABBA_1 | 153 | 158 | PF00400 | 0.636 |
LIG_eIF4E_1 | 116 | 122 | PF01652 | 0.493 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.504 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.504 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.585 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.701 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.580 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.595 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.699 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.547 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.686 |
LIG_Integrin_isoDGR_2 | 134 | 136 | PF01839 | 0.391 |
LIG_Integrin_isoDGR_2 | 160 | 162 | PF01839 | 0.423 |
LIG_Integrin_RGD_1 | 55 | 57 | PF01839 | 0.479 |
LIG_IRF3_LxIS_1 | 365 | 371 | PF10401 | 0.437 |
LIG_LIR_Gen_1 | 12 | 22 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 283 | 292 | PF02991 | 0.611 |
LIG_LIR_Gen_1 | 76 | 86 | PF02991 | 0.682 |
LIG_LIR_Nem_3 | 109 | 113 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 12 | 18 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 283 | 289 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 31 | 36 | PF02991 | 0.232 |
LIG_LIR_Nem_3 | 408 | 414 | PF02991 | 0.654 |
LIG_LIR_Nem_3 | 76 | 81 | PF02991 | 0.681 |
LIG_NRBOX | 118 | 124 | PF00104 | 0.567 |
LIG_OCRL_FandH_1 | 308 | 320 | PF00620 | 0.558 |
LIG_PCNA_PIPBox_1 | 279 | 288 | PF02747 | 0.548 |
LIG_PCNA_yPIPBox_3 | 157 | 167 | PF02747 | 0.614 |
LIG_PCNA_yPIPBox_3 | 279 | 288 | PF02747 | 0.492 |
LIG_PCNA_yPIPBox_3 | 294 | 308 | PF02747 | 0.556 |
LIG_Pex14_1 | 13 | 17 | PF04695 | 0.335 |
LIG_REV1ctd_RIR_1 | 379 | 387 | PF16727 | 0.562 |
LIG_SH2_CRK | 110 | 114 | PF00017 | 0.513 |
LIG_SH2_CRK | 116 | 120 | PF00017 | 0.497 |
LIG_SH2_GRB2like | 292 | 295 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.498 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.623 |
LIG_SUMO_SIM_par_1 | 24 | 31 | PF11976 | 0.246 |
LIG_SUMO_SIM_par_1 | 253 | 259 | PF11976 | 0.551 |
LIG_TRAF2_1 | 277 | 280 | PF00917 | 0.575 |
LIG_TYR_ITIM | 108 | 113 | PF00017 | 0.516 |
LIG_WW_3 | 204 | 208 | PF00397 | 0.570 |
MOD_CDC14_SPxK_1 | 204 | 207 | PF00782 | 0.585 |
MOD_CDK_SPK_2 | 63 | 68 | PF00069 | 0.699 |
MOD_CDK_SPxK_1 | 201 | 207 | PF00069 | 0.568 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.632 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.614 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.667 |
MOD_Cter_Amidation | 44 | 47 | PF01082 | 0.454 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.328 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.376 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.428 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.388 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.463 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.562 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.651 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.566 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.643 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.493 |
MOD_N-GLC_1 | 180 | 185 | PF02516 | 0.366 |
MOD_N-GLC_1 | 406 | 411 | PF02516 | 0.500 |
MOD_N-GLC_1 | 81 | 86 | PF02516 | 0.393 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.564 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.574 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.276 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.583 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.653 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.576 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.476 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.571 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.664 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.695 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.459 |
MOD_NEK2_2 | 269 | 274 | PF00069 | 0.643 |
MOD_PIKK_1 | 206 | 212 | PF00454 | 0.595 |
MOD_PIKK_1 | 238 | 244 | PF00454 | 0.636 |
MOD_PIKK_1 | 275 | 281 | PF00454 | 0.602 |
MOD_PIKK_1 | 335 | 341 | PF00454 | 0.651 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.612 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.630 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.453 |
MOD_PKB_1 | 47 | 55 | PF00069 | 0.644 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.599 |
MOD_Plk_1 | 406 | 412 | PF00069 | 0.673 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.646 |
MOD_Plk_1 | 81 | 87 | PF00069 | 0.558 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.494 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.614 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.589 |
MOD_Plk_4 | 386 | 392 | PF00069 | 0.599 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.650 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.686 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.646 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.528 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.533 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.634 |
TRG_DiLeu_BaEn_1 | 349 | 354 | PF01217 | 0.654 |
TRG_DiLeu_BaEn_2 | 15 | 21 | PF01217 | 0.411 |
TRG_DiLeu_BaEn_2 | 73 | 79 | PF01217 | 0.672 |
TRG_DiLeu_BaLyEn_6 | 227 | 232 | PF01217 | 0.484 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.522 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 392 | 395 | PF00928 | 0.652 |
TRG_ER_diArg_1 | 140 | 143 | PF00400 | 0.642 |
TRG_ER_diArg_1 | 312 | 315 | PF00400 | 0.588 |
TRG_ER_diArg_1 | 330 | 333 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 88 | 90 | PF00400 | 0.651 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKI4 | Leptomonas seymouri | 71% | 100% |
A0A1X0P177 | Trypanosomatidae | 49% | 100% |
A0A3Q8IBK9 | Leishmania donovani | 95% | 100% |
A0A3R7NQF7 | Trypanosoma rangeli | 49% | 100% |
A4HHK7 | Leishmania braziliensis | 82% | 100% |
A4I4R8 | Leishmania infantum | 95% | 100% |
E9ALL5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q17QW3 | Bos taurus | 26% | 100% |
Q9ERI6 | Mus musculus | 26% | 100% |
Q9HBH5 | Homo sapiens | 27% | 100% |
V5BBW8 | Trypanosoma cruzi | 49% | 100% |