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: A0A3S7WVT8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 48 | 52 | PF00656 | 0.584 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.710 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.710 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.679 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.776 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.620 |
DOC_CYCLIN_RxL_1 | 26 | 38 | PF00134 | 0.623 |
DOC_MAPK_gen_1 | 213 | 223 | PF00069 | 0.544 |
DOC_MAPK_gen_1 | 27 | 35 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 213 | 221 | PF00069 | 0.567 |
DOC_PP2B_LxvP_1 | 219 | 222 | PF13499 | 0.662 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.777 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.783 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.660 |
LIG_14-3-3_CanoR_1 | 150 | 156 | PF00244 | 0.661 |
LIG_14-3-3_CanoR_1 | 290 | 299 | PF00244 | 0.622 |
LIG_BIR_III_4 | 51 | 55 | PF00653 | 0.595 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.643 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.658 |
LIG_FHA_2 | 104 | 110 | PF00498 | 0.786 |
LIG_FHA_2 | 118 | 124 | PF00498 | 0.582 |
LIG_FHA_2 | 172 | 178 | PF00498 | 0.591 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.534 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.745 |
LIG_Pex14_2 | 114 | 118 | PF04695 | 0.802 |
LIG_SH2_CRK | 262 | 266 | PF00017 | 0.796 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.721 |
LIG_SH3_1 | 132 | 138 | PF00018 | 0.816 |
LIG_SH3_1 | 75 | 81 | PF00018 | 0.801 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.763 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.629 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.572 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.801 |
LIG_SUMO_SIM_par_1 | 31 | 38 | PF11976 | 0.522 |
LIG_TRAF2_1 | 10 | 13 | PF00917 | 0.555 |
LIG_WRC_WIRS_1 | 104 | 109 | PF05994 | 0.672 |
LIG_WW_3 | 134 | 138 | PF00397 | 0.734 |
MOD_CDC14_SPxK_1 | 312 | 315 | PF00782 | 0.646 |
MOD_CDK_SPK_2 | 309 | 314 | PF00069 | 0.672 |
MOD_CDK_SPxK_1 | 309 | 315 | PF00069 | 0.632 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.710 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.533 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.788 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.612 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.573 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.635 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.633 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.798 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.590 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.754 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.736 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.659 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.733 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.836 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.685 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.662 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.538 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.745 |
MOD_N-GLC_1 | 169 | 174 | PF02516 | 0.829 |
MOD_N-GLC_1 | 248 | 253 | PF02516 | 0.592 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.779 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.635 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.746 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.627 |
MOD_PKA_2 | 116 | 122 | PF00069 | 0.776 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.689 |
MOD_PKA_2 | 156 | 162 | PF00069 | 0.730 |
MOD_Plk_1 | 302 | 308 | PF00069 | 0.606 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.538 |
MOD_Plk_2-3 | 194 | 200 | PF00069 | 0.572 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.553 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.566 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.783 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.607 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.654 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.663 |
TRG_DiLeu_BaLyEn_6 | 230 | 235 | PF01217 | 0.536 |
TRG_ENDOCYTIC_2 | 262 | 265 | PF00928 | 0.803 |
TRG_ER_diArg_1 | 131 | 134 | PF00400 | 0.704 |
TRG_ER_diArg_1 | 230 | 233 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 30 | 32 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 313 | 315 | PF00400 | 0.791 |
TRG_Pf-PMV_PEXEL_1 | 31 | 36 | PF00026 | 0.514 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P529 | Leptomonas seymouri | 43% | 98% |
A4HYR9 | Leishmania infantum | 100% | 100% |
E9AI89 | Leishmania braziliensis | 67% | 100% |
E9AUH4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 98% |
Q4QD10 | Leishmania major | 90% | 100% |