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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A0A3Q8IL79
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 277 | 281 | PF00656 | 0.565 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.633 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.486 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.690 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.755 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.529 |
CLV_PCSK_PC1ET2_1 | 148 | 150 | PF00082 | 0.589 |
CLV_PCSK_PC1ET2_1 | 266 | 268 | PF00082 | 0.582 |
CLV_PCSK_PC1ET2_1 | 27 | 29 | PF00082 | 0.608 |
CLV_PCSK_PC1ET2_1 | 77 | 79 | PF00082 | 0.530 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.539 |
DOC_PP2B_LxvP_1 | 276 | 279 | PF13499 | 0.560 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.659 |
DOC_USP7_UBL2_3 | 234 | 238 | PF12436 | 0.638 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.664 |
LIG_14-3-3_CanoR_1 | 221 | 227 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 249 | 258 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 51 | 60 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 81 | 91 | PF00244 | 0.443 |
LIG_BIR_III_2 | 187 | 191 | PF00653 | 0.683 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.581 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.522 |
LIG_LIR_Gen_1 | 139 | 146 | PF02991 | 0.587 |
LIG_LIR_Gen_1 | 224 | 233 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 224 | 229 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 85 | 90 | PF02991 | 0.420 |
LIG_SH2_NCK_1 | 259 | 263 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 151 | 155 | PF00017 | 0.461 |
LIG_SH2_STAP1 | 259 | 263 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 87 | 91 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.537 |
LIG_SH3_1 | 77 | 83 | PF00018 | 0.505 |
LIG_SH3_3 | 189 | 195 | PF00018 | 0.619 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.489 |
LIG_TRAF2_1 | 252 | 255 | PF00917 | 0.583 |
MOD_CDK_SPxxK_3 | 141 | 148 | PF00069 | 0.524 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.536 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.621 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.536 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.545 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.699 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.512 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.548 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.527 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.439 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.625 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.553 |
MOD_Cter_Amidation | 234 | 237 | PF01082 | 0.634 |
MOD_Cter_Amidation | 25 | 28 | PF01082 | 0.664 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.643 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.703 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.451 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.723 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.586 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.615 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.420 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.587 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.563 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.654 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.452 |
MOD_N-GLC_1 | 249 | 254 | PF02516 | 0.569 |
MOD_N-GLC_1 | 46 | 51 | PF02516 | 0.716 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.507 |
MOD_NEK2_2 | 46 | 51 | PF00069 | 0.664 |
MOD_PIKK_1 | 194 | 200 | PF00454 | 0.593 |
MOD_PIKK_1 | 270 | 276 | PF00454 | 0.651 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.583 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.728 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.589 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.554 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.663 |
MOD_SUMO_rev_2 | 252 | 258 | PF00179 | 0.583 |
TRG_ER_diArg_1 | 75 | 78 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 80 | 82 | PF00400 | 0.492 |
TRG_NLS_MonoExtC_3 | 75 | 80 | PF00514 | 0.503 |
TRG_Pf-PMV_PEXEL_1 | 111 | 115 | PF00026 | 0.647 |
TRG_Pf-PMV_PEXEL_1 | 194 | 198 | PF00026 | 0.628 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAX4 | Leptomonas seymouri | 32% | 94% |
A4HC00 | Leishmania braziliensis | 60% | 99% |
A4HZE9 | Leishmania infantum | 99% | 100% |
E9AVD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QC43 | Leishmania major | 88% | 100% |