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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9B3U6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 134 | 138 | PF00656 | 0.643 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.518 |
CLV_PCSK_FUR_1 | 21 | 25 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.687 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.518 |
CLV_PCSK_PC1ET2_1 | 143 | 145 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 73 | 77 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.478 |
DEG_APCC_DBOX_1 | 100 | 108 | PF00400 | 0.462 |
DEG_APCC_DBOX_1 | 307 | 315 | PF00400 | 0.447 |
DEG_SPOP_SBC_1 | 179 | 183 | PF00917 | 0.678 |
DEG_SPOP_SBC_1 | 214 | 218 | PF00917 | 0.560 |
DEG_SPOP_SBC_1 | 51 | 55 | PF00917 | 0.522 |
DOC_CKS1_1 | 1 | 6 | PF01111 | 0.592 |
DOC_MAPK_gen_1 | 101 | 107 | PF00069 | 0.535 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.748 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.696 |
LIG_14-3-3_CanoR_1 | 23 | 33 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 283 | 287 | PF00244 | 0.608 |
LIG_14-3-3_CanoR_1 | 90 | 98 | PF00244 | 0.519 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.608 |
LIG_BRCT_BRCA1_1 | 230 | 234 | PF00533 | 0.464 |
LIG_BRCT_BRCA1_1 | 71 | 75 | PF00533 | 0.542 |
LIG_BRCT_BRCA1_2 | 230 | 236 | PF00533 | 0.601 |
LIG_CaM_IQ_9 | 77 | 92 | PF13499 | 0.415 |
LIG_LYPXL_yS_3 | 62 | 65 | PF13949 | 0.414 |
LIG_SH2_CRK | 242 | 246 | PF00017 | 0.617 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.675 |
LIG_SH3_2 | 201 | 206 | PF14604 | 0.477 |
LIG_SH3_2 | 39 | 44 | PF14604 | 0.462 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.484 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.523 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.533 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.607 |
LIG_SUMO_SIM_par_1 | 116 | 124 | PF11976 | 0.538 |
LIG_TRAF2_1 | 138 | 141 | PF00917 | 0.500 |
LIG_TRAF2_1 | 266 | 269 | PF00917 | 0.526 |
LIG_TYR_ITIM | 240 | 245 | PF00017 | 0.643 |
LIG_UBA3_1 | 104 | 110 | PF00899 | 0.525 |
LIG_UBA3_1 | 310 | 315 | PF00899 | 0.527 |
MOD_CDK_SPK_2 | 165 | 170 | PF00069 | 0.436 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.497 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.705 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.696 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.471 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.697 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.425 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.589 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.606 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.595 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.561 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.641 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.654 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.670 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.649 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.595 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.639 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.497 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.441 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.647 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.643 |
MOD_N-GLC_1 | 214 | 219 | PF02516 | 0.570 |
MOD_N-GLC_1 | 5 | 10 | PF02516 | 0.598 |
MOD_PIKK_1 | 110 | 116 | PF00454 | 0.415 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.431 |
MOD_PKA_2 | 258 | 264 | PF00069 | 0.690 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.513 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.535 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.522 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.622 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.596 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.491 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.690 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.552 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.691 |
MOD_SUMO_rev_2 | 291 | 300 | PF00179 | 0.484 |
MOD_SUMO_rev_2 | 99 | 104 | PF00179 | 0.472 |
TRG_DiLeu_BaEn_1 | 100 | 105 | PF01217 | 0.474 |
TRG_DiLeu_BaEn_1 | 306 | 311 | PF01217 | 0.503 |
TRG_DiLeu_BaLyEn_6 | 93 | 98 | PF01217 | 0.529 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.619 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.450 |
TRG_ER_diArg_1 | 282 | 284 | PF00400 | 0.557 |
TRG_NES_CRM1_1 | 116 | 131 | PF08389 | 0.539 |
TRG_Pf-PMV_PEXEL_1 | 308 | 312 | PF00026 | 0.479 |
TRG_Pf-PMV_PEXEL_1 | 315 | 319 | PF00026 | 0.545 |
TRG_Pf-PMV_PEXEL_1 | 96 | 100 | PF00026 | 0.532 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE12 | Leptomonas seymouri | 57% | 100% |
A0A0S4IXZ1 | Bodo saltans | 25% | 100% |
A0A1X0P0W7 | Trypanosomatidae | 38% | 100% |
A0A3R7NUE3 | Trypanosoma rangeli | 36% | 100% |
A0A3S7X6M7 | Leishmania donovani | 88% | 97% |
A4HLG6 | Leishmania braziliensis | 64% | 95% |
A4I8X7 | Leishmania infantum | 88% | 97% |
D0A4X5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
Q4Q478 | Leishmania major | 86% | 100% |