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 |
Related structures:
AlphaFold database: A4HYT3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 136 | 140 | PF00656 | 0.597 |
CLV_C14_Caspase3-7 | 260 | 264 | PF00656 | 0.674 |
CLV_MEL_PAP_1 | 30 | 36 | PF00089 | 0.419 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.473 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.680 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.395 |
CLV_PCSK_PC1ET2_1 | 103 | 105 | PF00082 | 0.680 |
CLV_PCSK_PC1ET2_1 | 84 | 86 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.470 |
DEG_APCC_DBOX_1 | 84 | 92 | PF00400 | 0.426 |
DEG_SPOP_SBC_1 | 179 | 183 | PF00917 | 0.684 |
DEG_SPOP_SBC_1 | 257 | 261 | PF00917 | 0.657 |
DOC_MAPK_MEF2A_6 | 55 | 62 | PF00069 | 0.498 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.730 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.677 |
LIG_14-3-3_CanoR_1 | 174 | 180 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 31 | 40 | PF00244 | 0.489 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.529 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.776 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.544 |
LIG_LIR_Gen_1 | 26 | 34 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 26 | 30 | PF02991 | 0.520 |
LIG_SH2_CRK | 80 | 84 | PF00017 | 0.506 |
LIG_SH2_STAT3 | 109 | 112 | PF00017 | 0.494 |
LIG_SH2_STAT3 | 69 | 72 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.520 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.602 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.646 |
LIG_SUMO_SIM_par_1 | 58 | 65 | PF11976 | 0.482 |
LIG_WRC_WIRS_1 | 24 | 29 | PF05994 | 0.462 |
LIG_WW_3 | 184 | 188 | PF00397 | 0.532 |
MOD_CDC14_SPxK_1 | 184 | 187 | PF00782 | 0.619 |
MOD_CDK_SPxK_1 | 181 | 187 | PF00069 | 0.625 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.529 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.594 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.725 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.687 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.555 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.608 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.693 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.490 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.661 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.684 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.607 |
MOD_GlcNHglycan | 132 | 136 | PF01048 | 0.628 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.677 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.518 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.573 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.710 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.591 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.524 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.659 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.715 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.632 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.593 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.754 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.570 |
MOD_N-GLC_1 | 116 | 121 | PF02516 | 0.475 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.718 |
MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.602 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.524 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.640 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.573 |
MOD_PIKK_1 | 226 | 232 | PF00454 | 0.637 |
MOD_PIKK_1 | 239 | 245 | PF00454 | 0.551 |
MOD_PIKK_1 | 68 | 74 | PF00454 | 0.467 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.575 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.432 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.484 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.443 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.532 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.477 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.529 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.625 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.679 |
MOD_SUMO_for_1 | 83 | 86 | PF00179 | 0.477 |
TRG_DiLeu_BaLyEn_6 | 17 | 22 | PF01217 | 0.463 |
TRG_DiLeu_BaLyEn_6 | 55 | 60 | PF01217 | 0.509 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.503 |
TRG_ER_diArg_1 | 172 | 174 | PF00400 | 0.565 |
TRG_ER_diArg_1 | 29 | 32 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 75 | 77 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 94 | 97 | PF00400 | 0.542 |
TRG_NLS_MonoExtN_4 | 100 | 107 | PF00514 | 0.485 |
TRG_Pf-PMV_PEXEL_1 | 97 | 101 | PF00026 | 0.490 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IBK6 | Leishmania donovani | 100% | 100% |
E9AIE2 | Leishmania braziliensis | 68% | 95% |
E9AUM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 95% |
Q4QCV5 | Leishmania major | 87% | 100% |