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: A0A3S7X6A3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 128 | 132 | PF00656 | 0.515 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.498 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.465 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.432 |
DEG_ODPH_VHL_1 | 172 | 185 | PF01847 | 0.514 |
DEG_SPOP_SBC_1 | 110 | 114 | PF00917 | 0.561 |
DEG_SPOP_SBC_1 | 19 | 23 | PF00917 | 0.538 |
DOC_MAPK_gen_1 | 39 | 48 | PF00069 | 0.543 |
DOC_PP1_RVXF_1 | 180 | 186 | PF00149 | 0.554 |
DOC_PP1_RVXF_1 | 204 | 210 | PF00149 | 0.579 |
DOC_PP4_FxxP_1 | 48 | 51 | PF00568 | 0.525 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.521 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.386 |
LIG_14-3-3_CanoR_1 | 85 | 94 | PF00244 | 0.495 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.493 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.585 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.482 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.361 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.429 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.456 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.455 |
LIG_LIR_Apic_2 | 276 | 280 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 155 | 160 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 21 | 27 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 245 | 251 | PF02991 | 0.438 |
LIG_PDZ_Class_2 | 356 | 361 | PF00595 | 0.512 |
LIG_SH2_NCK_1 | 127 | 131 | PF00017 | 0.476 |
LIG_SH2_SRC | 127 | 130 | PF00017 | 0.489 |
LIG_SH2_SRC | 137 | 140 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.495 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.495 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.555 |
LIG_SUMO_SIM_par_1 | 111 | 121 | PF11976 | 0.552 |
LIG_SUMO_SIM_par_1 | 281 | 287 | PF11976 | 0.491 |
LIG_SUMO_SIM_par_1 | 31 | 37 | PF11976 | 0.472 |
LIG_TRAF2_1 | 308 | 311 | PF00917 | 0.699 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.557 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.479 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.493 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.524 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.508 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.476 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.593 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.533 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.428 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.553 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.537 |
MOD_GlcNHglycan | 254 | 258 | PF01048 | 0.480 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.694 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.567 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.380 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.513 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.424 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.440 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.519 |
MOD_N-GLC_1 | 229 | 234 | PF02516 | 0.484 |
MOD_N-GLC_2 | 162 | 164 | PF02516 | 0.386 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.382 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.450 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.388 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.475 |
MOD_NEK2_2 | 246 | 251 | PF00069 | 0.524 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.463 |
MOD_Plk_2-3 | 93 | 99 | PF00069 | 0.560 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.412 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.461 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.393 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.529 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.382 |
TRG_DiLeu_BaEn_2 | 98 | 104 | PF01217 | 0.395 |
TRG_DiLeu_BaLyEn_6 | 179 | 184 | PF01217 | 0.547 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.411 |
TRG_ER_diArg_1 | 41 | 43 | PF00400 | 0.571 |
TRG_Pf-PMV_PEXEL_1 | 63 | 67 | PF00026 | 0.510 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3G5 | Leptomonas seymouri | 60% | 99% |
A0A1X0NS90 | Trypanosomatidae | 34% | 98% |
A0A3S5IR82 | Trypanosoma rangeli | 34% | 100% |
A4HL25 | Leishmania braziliensis | 83% | 100% |
A4I8K6 | Leishmania infantum | 100% | 100% |
D0AAK9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9B3G6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q4N4 | Leishmania major | 92% | 99% |
V5DE80 | Trypanosoma cruzi | 32% | 100% |