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 | yes | yes: 6, no: 1 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: A4HNM3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.531 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.628 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.610 |
DOC_CKS1_1 | 154 | 159 | PF01111 | 0.472 |
DOC_CYCLIN_yCln2_LP_2 | 154 | 160 | PF00134 | 0.511 |
DOC_MAPK_MEF2A_6 | 187 | 196 | PF00069 | 0.341 |
DOC_MAPK_MEF2A_6 | 94 | 103 | PF00069 | 0.501 |
DOC_MAPK_RevD_3 | 220 | 236 | PF00069 | 0.622 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.561 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.464 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.750 |
LIG_14-3-3_CanoR_1 | 199 | 207 | PF00244 | 0.386 |
LIG_Actin_WH2_2 | 88 | 104 | PF00022 | 0.566 |
LIG_Clathr_ClatBox_1 | 126 | 130 | PF01394 | 0.313 |
LIG_CtBP_PxDLS_1 | 96 | 100 | PF00389 | 0.391 |
LIG_EH1_1 | 128 | 136 | PF00400 | 0.486 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.480 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.320 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.481 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.537 |
LIG_LIR_Gen_1 | 118 | 129 | PF02991 | 0.425 |
LIG_LIR_LC3C_4 | 217 | 222 | PF02991 | 0.249 |
LIG_LIR_Nem_3 | 118 | 124 | PF02991 | 0.436 |
LIG_LYPXL_SIV_4 | 212 | 220 | PF13949 | 0.249 |
LIG_PDZ_Class_1 | 280 | 285 | PF00595 | 0.776 |
LIG_Pex14_1 | 120 | 124 | PF04695 | 0.334 |
LIG_SH2_CRK | 213 | 217 | PF00017 | 0.336 |
LIG_SH2_CRK | 82 | 86 | PF00017 | 0.489 |
LIG_SH2_NCK_1 | 213 | 217 | PF00017 | 0.311 |
LIG_SH2_SRC | 193 | 196 | PF00017 | 0.321 |
LIG_SH2_SRC | 213 | 216 | PF00017 | 0.249 |
LIG_SH2_STAP1 | 48 | 52 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.627 |
LIG_SH3_1 | 138 | 144 | PF00018 | 0.500 |
LIG_SH3_3 | 138 | 144 | PF00018 | 0.427 |
LIG_SUMO_SIM_anti_2 | 170 | 176 | PF11976 | 0.357 |
LIG_SUMO_SIM_anti_2 | 217 | 223 | PF11976 | 0.320 |
LIG_SUMO_SIM_par_1 | 170 | 176 | PF11976 | 0.397 |
LIG_TYR_ITIM | 80 | 85 | PF00017 | 0.621 |
LIG_UBA3_1 | 267 | 272 | PF00899 | 0.467 |
LIG_WRC_WIRS_1 | 126 | 131 | PF05994 | 0.630 |
LIG_WW_1 | 45 | 48 | PF00397 | 0.674 |
MOD_CDK_SPxK_1 | 153 | 159 | PF00069 | 0.661 |
MOD_CDK_SPxxK_3 | 250 | 257 | PF00069 | 0.697 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.492 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.640 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.631 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.699 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.721 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.646 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.625 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.647 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.492 |
MOD_N-GLC_1 | 149 | 154 | PF02516 | 0.523 |
MOD_N-GLC_1 | 250 | 255 | PF02516 | 0.488 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.484 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.544 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.628 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.599 |
MOD_NEK2_2 | 17 | 22 | PF00069 | 0.647 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.570 |
MOD_PKB_1 | 197 | 205 | PF00069 | 0.483 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.612 |
MOD_Plk_1 | 48 | 54 | PF00069 | 0.605 |
MOD_Plk_2-3 | 55 | 61 | PF00069 | 0.441 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.661 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.439 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.577 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.697 |
MOD_SUMO_for_1 | 271 | 274 | PF00179 | 0.539 |
TRG_DiLeu_BaEn_1 | 130 | 135 | PF01217 | 0.581 |
TRG_DiLeu_BaEn_1 | 170 | 175 | PF01217 | 0.469 |
TRG_DiLeu_BaLyEn_6 | 223 | 228 | PF01217 | 0.501 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.516 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.609 |
TRG_ER_diArg_1 | 137 | 139 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 196 | 199 | PF00400 | 0.532 |
TRG_Pf-PMV_PEXEL_1 | 22 | 26 | PF00026 | 0.447 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3B3 | Leptomonas seymouri | 44% | 99% |
A0A1X0P8Q0 | Trypanosomatidae | 25% | 100% |
A0A3Q8IN72 | Leishmania donovani | 79% | 100% |
A4ICX1 | Leishmania infantum | 79% | 100% |
E9ASD4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q4Q262 | Leishmania major | 76% | 100% |