Related to yeast azole resistance protein AZR1 and aspergullus citrate exporter CEX1.. Expanded on multiple lineages
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: 2 |
NetGPI | no | yes: 0, no: 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: A4H5K1
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 1 |
GO:0022857 | transmembrane transporter activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 340 | 342 | PF00675 | 0.499 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.346 |
DEG_MDM2_SWIB_1 | 135 | 142 | PF02201 | 0.400 |
DEG_SCF_FBW7_1 | 8 | 15 | PF00400 | 0.628 |
DOC_CDC14_PxL_1 | 322 | 330 | PF14671 | 0.753 |
DOC_CKS1_1 | 39 | 44 | PF01111 | 0.610 |
DOC_CYCLIN_RxL_1 | 156 | 164 | PF00134 | 0.544 |
DOC_CYCLIN_yCln2_LP_2 | 43 | 46 | PF00134 | 0.594 |
DOC_MAPK_gen_1 | 156 | 165 | PF00069 | 0.509 |
DOC_MAPK_MEF2A_6 | 144 | 151 | PF00069 | 0.383 |
DOC_MAPK_MEF2A_6 | 156 | 165 | PF00069 | 0.546 |
DOC_PP2B_LxvP_1 | 43 | 46 | PF13499 | 0.594 |
DOC_PP4_MxPP_1 | 80 | 83 | PF00568 | 0.593 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.376 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.611 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.628 |
LIG_14-3-3_CanoR_1 | 169 | 179 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 282 | 288 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 34 | 39 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 92 | 98 | PF00244 | 0.614 |
LIG_BIR_III_4 | 242 | 246 | PF00653 | 0.383 |
LIG_BRCT_BRCA1_1 | 183 | 187 | PF00533 | 0.391 |
LIG_BRCT_BRCA1_1 | 215 | 219 | PF00533 | 0.500 |
LIG_deltaCOP1_diTrp_1 | 137 | 143 | PF00928 | 0.395 |
LIG_deltaCOP1_diTrp_1 | 337 | 345 | PF00928 | 0.703 |
LIG_eIF4E_1 | 38 | 44 | PF01652 | 0.613 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.551 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.753 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.793 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.355 |
LIG_FHA_2 | 132 | 138 | PF00498 | 0.460 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.361 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.764 |
LIG_LIR_Apic_2 | 123 | 128 | PF02991 | 0.512 |
LIG_LIR_Apic_2 | 259 | 264 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 130 | 138 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 184 | 194 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 216 | 224 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 130 | 135 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 137 | 142 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 164 | 168 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 184 | 190 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 216 | 222 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 236 | 241 | PF02991 | 0.150 |
LIG_LIR_Nem_3 | 307 | 313 | PF02991 | 0.435 |
LIG_MYND_1 | 42 | 46 | PF01753 | 0.596 |
LIG_NRP_CendR_1 | 379 | 380 | PF00754 | 0.591 |
LIG_Pex14_1 | 121 | 125 | PF04695 | 0.539 |
LIG_Pex14_2 | 135 | 139 | PF04695 | 0.400 |
LIG_Pex14_2 | 183 | 187 | PF04695 | 0.483 |
LIG_Pex14_2 | 306 | 310 | PF04695 | 0.500 |
LIG_SH2_CRK | 261 | 265 | PF00017 | 0.453 |
LIG_SH2_CRK | 313 | 317 | PF00017 | 0.620 |
LIG_SH2_PTP2 | 148 | 151 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.668 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.553 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.761 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.541 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.593 |
LIG_SxIP_EBH_1 | 368 | 380 | PF03271 | 0.793 |
LIG_TRAF2_1 | 120 | 123 | PF00917 | 0.552 |
LIG_TRAF2_1 | 349 | 352 | PF00917 | 0.639 |
LIG_TYR_ITIM | 136 | 141 | PF00017 | 0.400 |
LIG_WRC_WIRS_1 | 162 | 167 | PF05994 | 0.542 |
LIG_WW_2 | 82 | 85 | PF00397 | 0.592 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.500 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.404 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.643 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.541 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.569 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.537 |
MOD_CK2_1 | 314 | 320 | PF00069 | 0.714 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.701 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.622 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.758 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.409 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.645 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.500 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.505 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.767 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.456 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.386 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.692 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.620 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.655 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.732 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.632 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.622 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.541 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.510 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.461 |
MOD_LATS_1 | 90 | 96 | PF00433 | 0.615 |
MOD_N-GLC_1 | 34 | 39 | PF02516 | 0.822 |
MOD_N-GLC_1 | 60 | 65 | PF02516 | 0.732 |
MOD_N-GLC_1 | 93 | 98 | PF02516 | 0.812 |
MOD_N-GLC_2 | 294 | 296 | PF02516 | 0.500 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.388 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.555 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.391 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.382 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.606 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.544 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.471 |
MOD_NEK2_2 | 110 | 115 | PF00069 | 0.374 |
MOD_NEK2_2 | 93 | 98 | PF00069 | 0.612 |
MOD_PIKK_1 | 344 | 350 | PF00454 | 0.681 |
MOD_PIKK_1 | 96 | 102 | PF00454 | 0.606 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.448 |
MOD_Plk_1 | 18 | 24 | PF00069 | 0.636 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.482 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.747 |
MOD_Plk_1 | 93 | 99 | PF00069 | 0.611 |
MOD_Plk_2-3 | 318 | 324 | PF00069 | 0.761 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.398 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.542 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.500 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.365 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.571 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.704 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.559 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.593 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.629 |
TRG_DiLeu_BaEn_4 | 351 | 357 | PF01217 | 0.747 |
TRG_DiLeu_BaLyEn_6 | 39 | 44 | PF01217 | 0.610 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.391 |
TRG_ER_diArg_1 | 338 | 341 | PF00400 | 0.699 |
TRG_ER_diArg_1 | 378 | 380 | PF00400 | 0.786 |
TRG_NES_CRM1_1 | 188 | 200 | PF08389 | 0.500 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NN50 | Trypanosomatidae | 41% | 75% |