Unique kinetoplastid membrane protein. Protein duplicated in Leishmanniids as well as in T. rangeli.
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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: E9AW75
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 104 | 106 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.738 |
CLV_PCSK_FUR_1 | 93 | 97 | PF00082 | 0.723 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.734 |
CLV_Separin_Metazoa | 102 | 106 | PF03568 | 0.478 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.345 |
DEG_SPOP_SBC_1 | 124 | 128 | PF00917 | 0.450 |
DOC_MAPK_gen_1 | 52 | 62 | PF00069 | 0.593 |
DOC_MAPK_MEF2A_6 | 55 | 64 | PF00069 | 0.490 |
DOC_PP4_FxxP_1 | 149 | 152 | PF00568 | 0.524 |
DOC_PP4_FxxP_1 | 195 | 198 | PF00568 | 0.480 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.619 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.381 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.515 |
LIG_14-3-3_CanoR_1 | 108 | 116 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 175 | 183 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 83 | 92 | PF00244 | 0.329 |
LIG_Actin_WH2_2 | 14 | 32 | PF00022 | 0.470 |
LIG_BIR_III_4 | 187 | 191 | PF00653 | 0.413 |
LIG_Clathr_ClatBox_1 | 71 | 75 | PF01394 | 0.470 |
LIG_DLG_GKlike_1 | 96 | 103 | PF00625 | 0.514 |
LIG_EH1_1 | 60 | 68 | PF00400 | 0.231 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.540 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.514 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.432 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.335 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.469 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.519 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.393 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.511 |
LIG_GBD_Chelix_1 | 17 | 25 | PF00786 | 0.533 |
LIG_IRF3_LxIS_1 | 59 | 65 | PF10401 | 0.327 |
LIG_LIR_Apic_2 | 147 | 152 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 35 | 41 | PF02991 | 0.699 |
LIG_LIR_Nem_3 | 35 | 39 | PF02991 | 0.701 |
LIG_SH2_NCK_1 | 9 | 13 | PF00017 | 0.470 |
LIG_SH2_SRC | 61 | 64 | PF00017 | 0.231 |
LIG_SH2_STAT3 | 258 | 261 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.533 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.406 |
LIG_SH3_3 | 195 | 201 | PF00018 | 0.515 |
LIG_SUMO_SIM_anti_2 | 120 | 128 | PF11976 | 0.502 |
LIG_SUMO_SIM_par_1 | 14 | 19 | PF11976 | 0.470 |
LIG_SUMO_SIM_par_1 | 69 | 76 | PF11976 | 0.467 |
LIG_TRAF2_1 | 252 | 255 | PF00917 | 0.531 |
LIG_TYR_ITIM | 59 | 64 | PF00017 | 0.295 |
LIG_WRC_WIRS_1 | 74 | 79 | PF05994 | 0.470 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.538 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.415 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.510 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.578 |
MOD_CK2_1 | 108 | 114 | PF00069 | 0.432 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.596 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.568 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.777 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.730 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.835 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.734 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.726 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.756 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.751 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.711 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.644 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.502 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.512 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.513 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.385 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.492 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.545 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.617 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.313 |
MOD_N-GLC_1 | 212 | 217 | PF02516 | 0.729 |
MOD_N-GLC_1 | 32 | 37 | PF02516 | 0.503 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.408 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.462 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.516 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.439 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.533 |
MOD_PKA_1 | 108 | 114 | PF00069 | 0.426 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.704 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.523 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.470 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.375 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.446 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.547 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.439 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.383 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.515 |
MOD_SUMO_rev_2 | 44 | 51 | PF00179 | 0.650 |
TRG_DiLeu_BaEn_4 | 255 | 261 | PF01217 | 0.408 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.375 |
TRG_ER_diArg_1 | 92 | 95 | PF00400 | 0.538 |
TRG_NLS_Bipartite_1 | 95 | 109 | PF00514 | 0.461 |
TRG_NLS_MonoExtC_3 | 104 | 109 | PF00514 | 0.478 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IBQ7 | Leishmania donovani | 82% | 100% |
A4H6G9 | Leishmania braziliensis | 64% | 100% |
A4I0B1 | Leishmania infantum | 82% | 100% |
Q9NF82 | Leishmania major | 78% | 100% |