A small folded protein with a long C-terminal TM segment. Very unclear topology.. Expanded on multiple lineages, especially Strigomonas.
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: 4, no: 9 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: Q4Q6L5
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0016491 | oxidoreductase activity | 2 | 2 |
GO:0016614 | oxidoreductase activity, acting on CH-OH group of donors | 3 | 2 |
GO:0016616 | oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.285 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 440 | 442 | PF00675 | 0.601 |
CLV_PCSK_FUR_1 | 23 | 27 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.299 |
CLV_PCSK_KEX2_1 | 462 | 464 | PF00082 | 0.648 |
CLV_PCSK_PC1ET2_1 | 214 | 216 | PF00082 | 0.306 |
CLV_PCSK_PC1ET2_1 | 281 | 283 | PF00082 | 0.285 |
CLV_PCSK_PC1ET2_1 | 462 | 464 | PF00082 | 0.666 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 469 | 473 | PF00082 | 0.677 |
CLV_PCSK_SKI1_1 | 76 | 80 | PF00082 | 0.227 |
DEG_APCC_DBOX_1 | 75 | 83 | PF00400 | 0.191 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.357 |
DOC_ANK_TNKS_1 | 440 | 447 | PF00023 | 0.377 |
DOC_CYCLIN_RxL_1 | 97 | 105 | PF00134 | 0.329 |
DOC_CYCLIN_yCln2_LP_2 | 6 | 12 | PF00134 | 0.191 |
DOC_MAPK_gen_1 | 89 | 99 | PF00069 | 0.331 |
DOC_MAPK_MEF2A_6 | 364 | 371 | PF00069 | 0.464 |
DOC_MAPK_MEF2A_6 | 92 | 101 | PF00069 | 0.307 |
DOC_PP2B_LxvP_1 | 6 | 9 | PF13499 | 0.191 |
DOC_PP4_FxxP_1 | 70 | 73 | PF00568 | 0.579 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.485 |
DOC_USP7_UBL2_3 | 214 | 218 | PF12436 | 0.437 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.364 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.589 |
LIG_14-3-3_CanoR_1 | 128 | 132 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 220 | 228 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 25 | 30 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 270 | 274 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 31 | 40 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 64 | 70 | PF00244 | 0.617 |
LIG_14-3-3_CanoR_1 | 83 | 91 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 92 | 99 | PF00244 | 0.387 |
LIG_Actin_WH2_2 | 113 | 130 | PF00022 | 0.341 |
LIG_APCC_ABBA_1 | 330 | 335 | PF00400 | 0.510 |
LIG_BRCT_BRCA1_1 | 298 | 302 | PF00533 | 0.411 |
LIG_BRCT_BRCA1_1 | 367 | 371 | PF00533 | 0.485 |
LIG_BRCT_BRCA1_1 | 416 | 420 | PF00533 | 0.297 |
LIG_BRCT_BRCA1_2 | 416 | 422 | PF00533 | 0.295 |
LIG_CaM_IQ_9 | 206 | 222 | PF13499 | 0.496 |
LIG_deltaCOP1_diTrp_1 | 353 | 361 | PF00928 | 0.489 |
LIG_eIF4E_1 | 184 | 190 | PF01652 | 0.496 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.347 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.533 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.507 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.565 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.354 |
LIG_FHA_2 | 191 | 197 | PF00498 | 0.485 |
LIG_IRF3_LxIS_1 | 206 | 212 | PF10401 | 0.485 |
LIG_LIR_Apic_2 | 18 | 24 | PF02991 | 0.191 |
LIG_LIR_Apic_2 | 69 | 73 | PF02991 | 0.580 |
LIG_LIR_Gen_1 | 142 | 147 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 161 | 169 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 222 | 233 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 142 | 146 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 161 | 165 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 353 | 358 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 368 | 374 | PF02991 | 0.489 |
LIG_MAD2 | 100 | 108 | PF02301 | 0.266 |
LIG_PCNA_yPIPBox_3 | 220 | 233 | PF02747 | 0.473 |
LIG_Pex14_1 | 198 | 202 | PF04695 | 0.496 |
LIG_Pex14_2 | 456 | 460 | PF04695 | 0.402 |
LIG_SH2_CRK | 162 | 166 | PF00017 | 0.456 |
LIG_SH2_CRK | 174 | 178 | PF00017 | 0.456 |
LIG_SH2_CRK | 184 | 188 | PF00017 | 0.496 |
LIG_SH2_SRC | 333 | 336 | PF00017 | 0.496 |
LIG_SH2_SRC | 374 | 377 | PF00017 | 0.496 |
LIG_SH2_STAP1 | 162 | 166 | PF00017 | 0.456 |
LIG_SH2_STAP1 | 174 | 178 | PF00017 | 0.456 |
LIG_SH2_STAP1 | 184 | 188 | PF00017 | 0.496 |
LIG_SH2_STAP1 | 202 | 206 | PF00017 | 0.496 |
LIG_SH2_STAP1 | 333 | 337 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 425 | 428 | PF00017 | 0.399 |
LIG_SH3_1 | 364 | 370 | PF00018 | 0.496 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.479 |
LIG_SH3_3 | 336 | 342 | PF00018 | 0.464 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.490 |
LIG_SUMO_SIM_anti_2 | 185 | 194 | PF11976 | 0.489 |
LIG_SUMO_SIM_par_1 | 185 | 194 | PF11976 | 0.489 |
LIG_TYR_ITIM | 172 | 177 | PF00017 | 0.411 |
MOD_CDK_SPK_2 | 26 | 31 | PF00069 | 0.589 |
MOD_CDK_SPxxK_3 | 111 | 118 | PF00069 | 0.364 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.535 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.519 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.431 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.189 |
MOD_CK2_1 | 446 | 452 | PF00069 | 0.538 |
MOD_CK2_1 | 467 | 473 | PF00069 | 0.461 |
MOD_CMANNOS | 45 | 48 | PF00535 | 0.379 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.265 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.267 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.385 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.621 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.379 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.247 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.535 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.538 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.542 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.434 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.509 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.520 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.401 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.405 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.197 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.489 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.442 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.485 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.547 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.535 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.396 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.390 |
MOD_NEK2_2 | 333 | 338 | PF00069 | 0.485 |
MOD_OFUCOSY | 11 | 16 | PF10250 | 0.191 |
MOD_PIKK_1 | 141 | 147 | PF00454 | 0.508 |
MOD_PIKK_1 | 219 | 225 | PF00454 | 0.480 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.591 |
MOD_PK_1 | 463 | 469 | PF00069 | 0.424 |
MOD_PKA_1 | 214 | 220 | PF00069 | 0.508 |
MOD_PKA_1 | 25 | 31 | PF00069 | 0.589 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.501 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.530 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.589 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.541 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.458 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.586 |
MOD_PKA_2 | 337 | 343 | PF00069 | 0.494 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.563 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.497 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.615 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.387 |
MOD_PKB_1 | 23 | 31 | PF00069 | 0.585 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.480 |
MOD_Plk_1 | 333 | 339 | PF00069 | 0.533 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.189 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.343 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.566 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.418 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.364 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.496 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.590 |
MOD_SUMO_rev_2 | 142 | 151 | PF00179 | 0.483 |
TRG_DiLeu_BaEn_1 | 142 | 147 | PF01217 | 0.481 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.496 |
TRG_ER_diArg_1 | 22 | 25 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 256 | 259 | PF00400 | 0.509 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P304 | Leptomonas seymouri | 26% | 100% |
A0A0N0P958 | Leptomonas seymouri | 61% | 100% |
A0A3Q8IGS5 | Leishmania donovani | 25% | 100% |
A0A3S7X466 | Leishmania donovani | 91% | 100% |
A4HJ26 | Leishmania braziliensis | 78% | 100% |
A4HLE0 | Leishmania braziliensis | 27% | 100% |
A4I6E8 | Leishmania infantum | 91% | 100% |
A4I8U9 | Leishmania infantum | 25% | 100% |
E8NHM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
E9B1J8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
E9B3R8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
Q4Q4A6 | Leishmania major | 26% | 100% |