Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 6 |
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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: E9AWB2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 150 | 154 | PF00656 | 0.346 |
CLV_C14_Caspase3-7 | 97 | 101 | PF00656 | 0.470 |
CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.446 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.445 |
CLV_PCSK_PC1ET2_1 | 148 | 150 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.521 |
DOC_MAPK_gen_1 | 191 | 200 | PF00069 | 0.591 |
DOC_MAPK_gen_1 | 203 | 211 | PF00069 | 0.373 |
DOC_MAPK_MEF2A_6 | 179 | 186 | PF00069 | 0.525 |
DOC_MAPK_MEF2A_6 | 203 | 211 | PF00069 | 0.395 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.323 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.560 |
DOC_USP7_UBL2_3 | 11 | 15 | PF12436 | 0.475 |
DOC_USP7_UBL2_3 | 125 | 129 | PF12436 | 0.443 |
DOC_USP7_UBL2_3 | 144 | 148 | PF12436 | 0.589 |
DOC_USP7_UBL2_3 | 158 | 162 | PF12436 | 0.427 |
DOC_USP7_UBL2_3 | 171 | 175 | PF12436 | 0.474 |
LIG_14-3-3_CanoR_1 | 203 | 211 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 216 | 223 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 67 | 73 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 92 | 99 | PF00244 | 0.715 |
LIG_Actin_WH2_2 | 110 | 127 | PF00022 | 0.544 |
LIG_APCC_Cbox_2 | 73 | 79 | PF00515 | 0.563 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.436 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.524 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.560 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.513 |
LIG_LIR_Gen_1 | 195 | 201 | PF02991 | 0.617 |
LIG_LIR_Gen_1 | 220 | 230 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 103 | 109 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 195 | 200 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 220 | 226 | PF02991 | 0.483 |
LIG_SH2_CRK | 197 | 201 | PF00017 | 0.434 |
LIG_SH2_NCK_1 | 24 | 28 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 24 | 28 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.452 |
LIG_TRAF2_1 | 136 | 139 | PF00917 | 0.338 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.564 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.430 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.509 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.617 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.542 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.404 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.676 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.528 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.539 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.493 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.462 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.463 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.581 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.749 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.549 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.507 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.548 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.523 |
MOD_N-GLC_1 | 162 | 167 | PF02516 | 0.438 |
MOD_N-GLC_1 | 87 | 92 | PF02516 | 0.670 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.519 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.446 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.626 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.645 |
MOD_PIKK_1 | 202 | 208 | PF00454 | 0.506 |
MOD_PIKK_1 | 50 | 56 | PF00454 | 0.546 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.522 |
MOD_PK_1 | 162 | 168 | PF00069 | 0.399 |
MOD_PKA_1 | 147 | 153 | PF00069 | 0.562 |
MOD_PKA_1 | 15 | 21 | PF00069 | 0.460 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.467 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.665 |
MOD_Plk_1 | 162 | 168 | PF00069 | 0.399 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.513 |
MOD_Plk_1 | 94 | 100 | PF00069 | 0.527 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.538 |
MOD_SUMO_rev_2 | 118 | 127 | PF00179 | 0.526 |
MOD_SUMO_rev_2 | 150 | 160 | PF00179 | 0.577 |
MOD_SUMO_rev_2 | 4 | 13 | PF00179 | 0.576 |
TRG_DiLeu_BaEn_1 | 196 | 201 | PF01217 | 0.577 |
TRG_DiLeu_BaEn_1 | 9 | 14 | PF01217 | 0.569 |
TRG_ENDOCYTIC_2 | 197 | 200 | PF00928 | 0.520 |
TRG_ENDOCYTIC_2 | 223 | 226 | PF00928 | 0.550 |
TRG_Pf-PMV_PEXEL_1 | 50 | 54 | PF00026 | 0.531 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCG3 | Leptomonas seymouri | 51% | 99% |
A0A1X0NYD1 | Trypanosomatidae | 30% | 90% |
A0A3Q8ICK8 | Leishmania donovani | 78% | 100% |
A0A3R7KGK2 | Trypanosoma rangeli | 28% | 100% |
A4HCW9 | Leishmania braziliensis | 61% | 100% |
A4I0E9 | Leishmania infantum | 78% | 100% |
Q4QB63 | Leishmania major | 78% | 100% |