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: E9AUH4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 284 | 288 | PF00656 | 0.471 |
CLV_C14_Caspase3-7 | 53 | 57 | PF00656 | 0.550 |
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 280 | 282 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.597 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.695 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.502 |
DEG_COP1_1 | 116 | 127 | PF00400 | 0.510 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.525 |
DOC_CYCLIN_RxL_1 | 26 | 38 | PF00134 | 0.518 |
DOC_MAPK_gen_1 | 208 | 218 | PF00069 | 0.444 |
DOC_MAPK_gen_1 | 27 | 35 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 211 | 218 | PF00069 | 0.470 |
DOC_MAPK_NFAT4_5 | 211 | 219 | PF00069 | 0.352 |
DOC_PP2B_LxvP_1 | 214 | 217 | PF13499 | 0.547 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.524 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.732 |
LIG_14-3-3_CanoR_1 | 113 | 122 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 146 | 151 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 208 | 218 | PF00244 | 0.356 |
LIG_14-3-3_CanoR_1 | 98 | 104 | PF00244 | 0.529 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.540 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.580 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.686 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.653 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.489 |
LIG_FHA_2 | 282 | 288 | PF00498 | 0.454 |
LIG_FHA_2 | 51 | 57 | PF00498 | 0.503 |
LIG_LIR_Gen_1 | 143 | 150 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 143 | 147 | PF02991 | 0.554 |
LIG_Pex14_2 | 110 | 114 | PF04695 | 0.685 |
LIG_SH2_CRK | 258 | 262 | PF00017 | 0.640 |
LIG_SH2_STAT3 | 63 | 66 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.613 |
LIG_SH3_1 | 128 | 134 | PF00018 | 0.704 |
LIG_SH3_1 | 75 | 81 | PF00018 | 0.705 |
LIG_SH3_3 | 119 | 125 | PF00018 | 0.583 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.634 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.544 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.717 |
LIG_SUMO_SIM_par_1 | 31 | 38 | PF11976 | 0.453 |
LIG_TRAF2_1 | 10 | 13 | PF00917 | 0.464 |
LIG_WW_3 | 130 | 134 | PF00397 | 0.648 |
MOD_CDC14_SPxK_1 | 308 | 311 | PF00782 | 0.525 |
MOD_CDK_SPK_2 | 305 | 310 | PF00069 | 0.566 |
MOD_CDK_SPxK_1 | 305 | 311 | PF00069 | 0.516 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.690 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.460 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.495 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.527 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.779 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.686 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.786 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.518 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.708 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.585 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.399 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.536 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.496 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.777 |
MOD_N-GLC_1 | 164 | 169 | PF02516 | 0.703 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.585 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.599 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.533 |
MOD_PIKK_1 | 231 | 237 | PF00454 | 0.392 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.580 |
MOD_PKB_1 | 96 | 104 | PF00069 | 0.523 |
MOD_Plk_1 | 286 | 292 | PF00069 | 0.496 |
MOD_Plk_1 | 298 | 304 | PF00069 | 0.486 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.448 |
MOD_Plk_2-3 | 189 | 195 | PF00069 | 0.496 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.496 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.492 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.515 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.551 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.734 |
TRG_DiLeu_BaLyEn_6 | 225 | 230 | PF01217 | 0.464 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.634 |
TRG_ER_diArg_1 | 127 | 129 | PF00400 | 0.618 |
TRG_ER_diArg_1 | 225 | 228 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 30 | 32 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 309 | 311 | PF00400 | 0.593 |
TRG_ER_diArg_1 | 95 | 98 | PF00400 | 0.514 |
TRG_Pf-PMV_PEXEL_1 | 31 | 36 | PF00026 | 0.515 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P529 | Leptomonas seymouri | 43% | 97% |
A0A3S7WVT8 | Leishmania donovani | 85% | 99% |
A4HYR9 | Leishmania infantum | 85% | 99% |
E9AI89 | Leishmania braziliensis | 65% | 100% |
Q4QD10 | Leishmania major | 80% | 100% |