Uncharacterized Protein, Uncharacterized
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | yes | yes: 4 |
Forrest at al. (procyclic) | no | yes: 2 |
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: 22 |
NetGPI | no | yes: 0, no: 22 |
Related structures:
AlphaFold database: E9AHL0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 203 | 207 | PF00656 | 0.509 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.465 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.436 |
CLV_PCSK_PC1ET2_1 | 191 | 193 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.632 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.538 |
DOC_MAPK_gen_1 | 157 | 164 | PF00069 | 0.485 |
DOC_PP4_FxxP_1 | 7 | 10 | PF00568 | 0.538 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.504 |
DOC_USP7_UBL2_3 | 103 | 107 | PF12436 | 0.442 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.734 |
LIG_14-3-3_CanoR_1 | 230 | 234 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 283 | 289 | PF00244 | 0.585 |
LIG_Actin_WH2_2 | 88 | 105 | PF00022 | 0.481 |
LIG_AP2alpha_1 | 171 | 175 | PF02296 | 0.458 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.658 |
LIG_BRCT_BRCA1_1 | 47 | 51 | PF00533 | 0.483 |
LIG_BRCT_BRCA1_1 | 55 | 59 | PF00533 | 0.516 |
LIG_CaM_IQ_9 | 161 | 176 | PF13499 | 0.331 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.467 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.485 |
LIG_FHA_2 | 58 | 64 | PF00498 | 0.457 |
LIG_LIR_Apic_2 | 6 | 10 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 172 | 182 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 48 | 59 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 118 | 123 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 172 | 178 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 25 | 29 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 48 | 54 | PF02991 | 0.467 |
LIG_Pex14_2 | 171 | 175 | PF04695 | 0.431 |
LIG_Rb_LxCxE_1 | 216 | 235 | PF01857 | 0.396 |
LIG_SH2_CRK | 87 | 91 | PF00017 | 0.449 |
LIG_SH2_SRC | 67 | 70 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.472 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.434 |
LIG_SUMO_SIM_anti_2 | 243 | 249 | PF11976 | 0.396 |
LIG_TRAF2_1 | 214 | 217 | PF00917 | 0.483 |
LIG_TRAF2_2 | 10 | 15 | PF00917 | 0.498 |
LIG_TRFH_1 | 254 | 258 | PF08558 | 0.538 |
LIG_UBA3_1 | 33 | 38 | PF00899 | 0.516 |
LIG_WRC_WIRS_1 | 23 | 28 | PF05994 | 0.485 |
LIG_WW_3 | 292 | 296 | PF00397 | 0.576 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.539 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.549 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.635 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.659 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.546 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.436 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.474 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.633 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.587 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.412 |
MOD_GlcNHglycan | 116 | 120 | PF01048 | 0.401 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.525 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.471 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.694 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.600 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.538 |
MOD_N-GLC_1 | 183 | 188 | PF02516 | 0.562 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.471 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.518 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.490 |
MOD_PIKK_1 | 248 | 254 | PF00454 | 0.516 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.487 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.708 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.628 |
MOD_Plk_1 | 243 | 249 | PF00069 | 0.682 |
MOD_Plk_2-3 | 74 | 80 | PF00069 | 0.361 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.470 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.558 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.593 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.736 |
MOD_SUMO_for_1 | 113 | 116 | PF00179 | 0.502 |
TRG_DiLeu_BaEn_4 | 216 | 222 | PF01217 | 0.515 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.479 |
TRG_ER_diArg_1 | 294 | 297 | PF00400 | 0.584 |
TRG_NLS_MonoExtN_4 | 122 | 128 | PF00514 | 0.491 |
TRG_Pf-PMV_PEXEL_1 | 104 | 108 | PF00026 | 0.598 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P348 | Leptomonas seymouri | 24% | 71% |
A0A0N0P3S1 | Leptomonas seymouri | 60% | 68% |
A0A0N0P4S1 | Leptomonas seymouri | 23% | 100% |
A0A1X0NK28 | Trypanosomatidae | 38% | 76% |
A0A3Q8IG21 | Leishmania donovani | 94% | 74% |
A0A3Q8IIE7 | Leishmania donovani | 98% | 100% |
A0A3S5H792 | Leishmania donovani | 24% | 100% |
A0A3S7WQB3 | Leishmania donovani | 25% | 74% |
A4H6C6 | Leishmania braziliensis | 23% | 100% |
A4HJ56 | Leishmania braziliensis | 68% | 100% |
A4HTM7 | Leishmania infantum | 25% | 74% |
A4HZL5 | Leishmania infantum | 24% | 100% |
A4I6H9 | Leishmania infantum | 93% | 100% |
E9AMG1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 74% |
E9B1M8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
E9B1N5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
E9B1N6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
Q4Q6H8 | Leishmania major | 82% | 100% |
Q4Q6I6 | Leishmania major | 79% | 99% |
Q4QCL3 | Leishmania major | 25% | 100% |
Q4QI82 | Leishmania major | 24% | 100% |