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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: E9AX45
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 141 | 145 | PF00656 | 0.519 |
CLV_C14_Caspase3-7 | 236 | 240 | PF00656 | 0.459 |
CLV_C14_Caspase3-7 | 256 | 260 | PF00656 | 0.606 |
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.560 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.356 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 340 | 344 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.449 |
DOC_MAPK_MEF2A_6 | 302 | 309 | PF00069 | 0.590 |
DOC_PP1_RVXF_1 | 338 | 344 | PF00149 | 0.338 |
DOC_PP1_RVXF_1 | 5 | 11 | PF00149 | 0.604 |
DOC_PP2B_LxvP_1 | 332 | 335 | PF13499 | 0.531 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.460 |
LIG_14-3-3_CanoR_1 | 213 | 220 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 221 | 226 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 254 | 258 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 320 | 328 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 37 | 41 | PF00244 | 0.326 |
LIG_14-3-3_CanoR_1 | 95 | 100 | PF00244 | 0.544 |
LIG_BIR_III_4 | 247 | 251 | PF00653 | 0.614 |
LIG_FHA_2 | 234 | 240 | PF00498 | 0.449 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.472 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.518 |
LIG_LIR_Gen_1 | 261 | 271 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.531 |
LIG_Pex14_1 | 180 | 184 | PF04695 | 0.700 |
LIG_SH2_CRK | 3 | 7 | PF00017 | 0.529 |
LIG_SH2_GRB2like | 16 | 19 | PF00017 | 0.570 |
LIG_SH2_NCK_1 | 57 | 61 | PF00017 | 0.400 |
LIG_SH2_SRC | 123 | 126 | PF00017 | 0.523 |
LIG_SH2_STAP1 | 16 | 20 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.561 |
LIG_SH3_1 | 165 | 171 | PF00018 | 0.506 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.559 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.604 |
LIG_SH3_3 | 316 | 322 | PF00018 | 0.634 |
LIG_TRAF2_1 | 42 | 45 | PF00917 | 0.416 |
LIG_WW_3 | 210 | 214 | PF00397 | 0.394 |
LIG_WW_3 | 320 | 324 | PF00397 | 0.470 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.540 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.613 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.438 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.557 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.384 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.512 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.532 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.501 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.585 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.608 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.599 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.362 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.593 |
MOD_GlcNHglycan | 247 | 251 | PF01048 | 0.756 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.301 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.345 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.578 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.547 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.714 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.699 |
MOD_LATS_1 | 36 | 42 | PF00433 | 0.324 |
MOD_N-GLC_1 | 330 | 335 | PF02516 | 0.576 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.660 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.664 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.659 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.640 |
MOD_PIKK_1 | 233 | 239 | PF00454 | 0.505 |
MOD_PK_1 | 30 | 36 | PF00069 | 0.524 |
MOD_PKA_1 | 95 | 101 | PF00069 | 0.684 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.467 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.790 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.573 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.372 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.696 |
MOD_PKB_1 | 95 | 103 | PF00069 | 0.546 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.565 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.482 |
MOD_Plk_2-3 | 330 | 336 | PF00069 | 0.583 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.560 |
MOD_SUMO_for_1 | 81 | 84 | PF00179 | 0.467 |
MOD_SUMO_rev_2 | 141 | 148 | PF00179 | 0.499 |
TRG_DiLeu_BaEn_4 | 71 | 77 | PF01217 | 0.510 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.549 |
TRG_ER_diArg_1 | 107 | 110 | PF00400 | 0.362 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 87 | 89 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 95 | 97 | PF00400 | 0.464 |
TRG_Pf-PMV_PEXEL_1 | 79 | 83 | PF00026 | 0.365 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3P5 | Leptomonas seymouri | 54% | 100% |
A0A3Q8ID13 | Leishmania donovani | 87% | 100% |
A0A422NWQ4 | Trypanosoma rangeli | 33% | 100% |
A4HDR1 | Leishmania braziliensis | 73% | 99% |
A4I107 | Leishmania infantum | 89% | 100% |
C9ZWA2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
Q4QAD1 | Leishmania major | 91% | 100% |
V5BJJ9 | Trypanosoma cruzi | 35% | 100% |