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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AIE2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 195 | 199 | PF00656 | 0.518 |
CLV_C14_Caspase3-7 | 247 | 251 | PF00656 | 0.688 |
CLV_MEL_PAP_1 | 30 | 36 | PF00089 | 0.360 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.384 |
CLV_PCSK_FUR_1 | 101 | 105 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.384 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.408 |
CLV_PCSK_PC1ET2_1 | 103 | 105 | PF00082 | 0.654 |
CLV_PCSK_PC1ET2_1 | 214 | 216 | PF00082 | 0.545 |
CLV_PCSK_PC1ET2_1 | 223 | 225 | PF00082 | 0.587 |
CLV_PCSK_PC1ET2_1 | 84 | 86 | PF00082 | 0.408 |
CLV_PCSK_PC7_1 | 226 | 232 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.389 |
DEG_SPOP_SBC_1 | 155 | 159 | PF00917 | 0.510 |
DEG_SPOP_SBC_1 | 179 | 183 | PF00917 | 0.671 |
DOC_CDC14_PxL_1 | 54 | 62 | PF14671 | 0.430 |
DOC_MAPK_MEF2A_6 | 55 | 62 | PF00069 | 0.406 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.727 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.645 |
LIG_14-3-3_CanoR_1 | 31 | 40 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 75 | 81 | PF00244 | 0.289 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.423 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.507 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.760 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.395 |
LIG_LIR_Gen_1 | 26 | 34 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 26 | 30 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 79 | 83 | PF02991 | 0.325 |
LIG_SH2_CRK | 80 | 84 | PF00017 | 0.395 |
LIG_SH2_STAT3 | 109 | 112 | PF00017 | 0.464 |
LIG_SH2_STAT3 | 69 | 72 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.445 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.658 |
LIG_SUMO_SIM_par_1 | 13 | 19 | PF11976 | 0.340 |
LIG_SUMO_SIM_par_1 | 58 | 65 | PF11976 | 0.384 |
LIG_TRAF2_1 | 207 | 210 | PF00917 | 0.542 |
LIG_WRC_WIRS_1 | 24 | 29 | PF05994 | 0.369 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.423 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.598 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.630 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.664 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.394 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.608 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.559 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.542 |
MOD_GlcNHglycan | 132 | 136 | PF01048 | 0.584 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.621 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.605 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.601 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.617 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.693 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.770 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.632 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.619 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.567 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.624 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.429 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.707 |
MOD_N-GLC_1 | 226 | 231 | PF02516 | 0.588 |
MOD_N-GLC_1 | 253 | 258 | PF02516 | 0.504 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.428 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.403 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.370 |
MOD_PIKK_1 | 183 | 189 | PF00454 | 0.523 |
MOD_PIKK_1 | 68 | 74 | PF00454 | 0.381 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.562 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.563 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.375 |
MOD_PKB_1 | 224 | 232 | PF00069 | 0.534 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.436 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.585 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.380 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.500 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.645 |
MOD_SUMO_for_1 | 83 | 86 | PF00179 | 0.398 |
MOD_SUMO_rev_2 | 194 | 202 | PF00179 | 0.545 |
TRG_DiLeu_BaLyEn_6 | 17 | 22 | PF01217 | 0.443 |
TRG_DiLeu_BaLyEn_6 | 55 | 60 | PF01217 | 0.419 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.391 |
TRG_ER_diArg_1 | 29 | 32 | PF00400 | 0.375 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 75 | 77 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 94 | 97 | PF00400 | 0.424 |
TRG_NLS_Bipartite_1 | 213 | 227 | PF00514 | 0.543 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P637 | Leptomonas seymouri | 48% | 100% |
A0A3Q8IBK6 | Leishmania donovani | 68% | 95% |
A4HYT3 | Leishmania infantum | 68% | 95% |
E9AUM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 100% |
Q4QCV5 | Leishmania major | 66% | 100% |