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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A4I8X7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 145 | 149 | PF00656 | 0.494 |
CLV_C14_Caspase3-7 | 27 | 31 | PF00656 | 0.539 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.520 |
CLV_PCSK_FUR_1 | 21 | 25 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.547 |
CLV_PCSK_PC1ET2_1 | 154 | 156 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.413 |
DEG_APCC_DBOX_1 | 111 | 119 | PF00400 | 0.429 |
DEG_APCC_DBOX_1 | 318 | 326 | PF00400 | 0.460 |
DEG_SPOP_SBC_1 | 190 | 194 | PF00917 | 0.636 |
DEG_SPOP_SBC_1 | 225 | 229 | PF00917 | 0.507 |
DOC_CKS1_1 | 1 | 6 | PF01111 | 0.570 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.609 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.743 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.662 |
LIG_14-3-3_CanoR_1 | 101 | 109 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 23 | 33 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 294 | 298 | PF00244 | 0.511 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.629 |
LIG_BRCT_BRCA1_1 | 241 | 245 | PF00533 | 0.492 |
LIG_BRCT_BRCA1_1 | 42 | 46 | PF00533 | 0.530 |
LIG_BRCT_BRCA1_1 | 82 | 86 | PF00533 | 0.517 |
LIG_BRCT_BRCA1_2 | 241 | 247 | PF00533 | 0.580 |
LIG_CaM_IQ_9 | 88 | 103 | PF13499 | 0.426 |
LIG_LIR_Nem_3 | 43 | 49 | PF02991 | 0.527 |
LIG_SH2_CRK | 253 | 257 | PF00017 | 0.608 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.635 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.756 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.558 |
LIG_SUMO_SIM_par_1 | 127 | 134 | PF11976 | 0.502 |
LIG_TRAF2_1 | 149 | 152 | PF00917 | 0.503 |
LIG_TYR_ITIM | 251 | 256 | PF00017 | 0.609 |
LIG_UBA3_1 | 115 | 121 | PF00899 | 0.516 |
LIG_UBA3_1 | 321 | 326 | PF00899 | 0.513 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.575 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.512 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.664 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.621 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.634 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.511 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.562 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.624 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.585 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.489 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.648 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.781 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.589 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.681 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.711 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.611 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.658 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.643 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.533 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.482 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.664 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.622 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.616 |
MOD_N-GLC_1 | 225 | 230 | PF02516 | 0.531 |
MOD_N-GLC_1 | 6 | 11 | PF02516 | 0.611 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.423 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.475 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.674 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.517 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.587 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.370 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.595 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.745 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.659 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.765 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.655 |
MOD_SUMO_rev_2 | 27 | 34 | PF00179 | 0.540 |
MOD_SUMO_rev_2 | 302 | 311 | PF00179 | 0.576 |
TRG_DiLeu_BaEn_1 | 111 | 116 | PF01217 | 0.483 |
TRG_DiLeu_BaEn_1 | 317 | 322 | PF01217 | 0.468 |
TRG_DiLeu_BaLyEn_6 | 104 | 109 | PF01217 | 0.503 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.568 |
TRG_ER_diArg_1 | 293 | 295 | PF00400 | 0.517 |
TRG_NES_CRM1_1 | 127 | 142 | PF08389 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 107 | 111 | PF00026 | 0.542 |
TRG_Pf-PMV_PEXEL_1 | 319 | 323 | PF00026 | 0.499 |
TRG_Pf-PMV_PEXEL_1 | 326 | 330 | PF00026 | 0.448 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE12 | Leptomonas seymouri | 58% | 100% |
A0A1X0P0W7 | Trypanosomatidae | 39% | 100% |
A0A3S7X6M7 | Leishmania donovani | 98% | 100% |
A4HLG6 | Leishmania braziliensis | 75% | 100% |
D0A4X5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9B3U6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 97% |
Q4Q478 | Leishmania major | 92% | 100% |