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. | yes | yes: 5 |
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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: Q4QIA5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.513 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.680 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.639 |
DEG_SCF_FBW7_2 | 55 | 61 | PF00400 | 0.390 |
DOC_CKS1_1 | 55 | 60 | PF01111 | 0.390 |
DOC_CYCLIN_RxL_1 | 176 | 186 | PF00134 | 0.483 |
DOC_MAPK_MEF2A_6 | 190 | 198 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 204 | 213 | PF00069 | 0.400 |
DOC_MAPK_MEF2A_6 | 71 | 80 | PF00069 | 0.394 |
DOC_PP2B_LxvP_1 | 175 | 178 | PF13499 | 0.428 |
DOC_PP2B_LxvP_1 | 209 | 212 | PF13499 | 0.434 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.335 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.353 |
DOC_USP7_UBL2_3 | 67 | 71 | PF12436 | 0.436 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.384 |
LIG_14-3-3_CanoR_1 | 111 | 115 | PF00244 | 0.687 |
LIG_14-3-3_CanoR_1 | 276 | 283 | PF00244 | 0.661 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.609 |
LIG_deltaCOP1_diTrp_1 | 248 | 254 | PF00928 | 0.425 |
LIG_EH_1 | 229 | 233 | PF12763 | 0.389 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.474 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.539 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.561 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.477 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.473 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.273 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.475 |
LIG_LIR_Gen_1 | 101 | 109 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 252 | 262 | PF02991 | 0.324 |
LIG_LIR_LC3C_4 | 267 | 271 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 101 | 106 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 252 | 257 | PF02991 | 0.361 |
LIG_SH2_GRB2like | 146 | 149 | PF00017 | 0.399 |
LIG_SH2_NCK_1 | 56 | 60 | PF00017 | 0.380 |
LIG_SH2_STAP1 | 146 | 150 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.397 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.458 |
LIG_SUMO_SIM_anti_2 | 267 | 275 | PF11976 | 0.408 |
LIG_SUMO_SIM_anti_2 | 285 | 292 | PF11976 | 0.592 |
LIG_SUMO_SIM_anti_2 | 5 | 13 | PF11976 | 0.625 |
LIG_SUMO_SIM_par_1 | 267 | 275 | PF11976 | 0.391 |
LIG_UBA3_1 | 208 | 215 | PF00899 | 0.435 |
LIG_WRC_WIRS_1 | 106 | 111 | PF05994 | 0.621 |
LIG_WRC_WIRS_1 | 236 | 241 | PF05994 | 0.452 |
LIG_WRC_WIRS_1 | 66 | 71 | PF05994 | 0.376 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.674 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.659 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.694 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.360 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.447 |
MOD_DYRK1A_RPxSP_1 | 190 | 194 | PF00069 | 0.430 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.278 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.317 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.394 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.440 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.278 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.550 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.657 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.443 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.453 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.550 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.394 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.412 |
MOD_N-GLC_1 | 153 | 158 | PF02516 | 0.699 |
MOD_N-GLC_1 | 42 | 47 | PF02516 | 0.629 |
MOD_N-GLC_2 | 149 | 151 | PF02516 | 0.624 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.657 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.620 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.484 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.475 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.263 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.385 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.664 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.322 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.465 |
MOD_NEK2_2 | 235 | 240 | PF00069 | 0.445 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.375 |
MOD_PKA_1 | 276 | 282 | PF00069 | 0.678 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.655 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.676 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.492 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.424 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.502 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.462 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.457 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.340 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.471 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.429 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.501 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.384 |
TRG_DiLeu_BaEn_1 | 294 | 299 | PF01217 | 0.692 |
TRG_DiLeu_LyEn_5 | 294 | 299 | PF01217 | 0.718 |
TRG_ER_diArg_1 | 114 | 117 | PF00400 | 0.698 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I287 | Leptomonas seymouri | 38% | 100% |
A0A3S7WQ88 | Leishmania donovani | 82% | 100% |
A4H5G2 | Leishmania braziliensis | 58% | 100% |
A4HTL2 | Leishmania infantum | 81% | 100% |
E9AME3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 98% |