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: A0A3S7X926
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 201 | 205 | PF00656 | 0.638 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.621 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.621 |
CLV_PCSK_PC7_1 | 47 | 53 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.743 |
DEG_SCF_FBW7_1 | 191 | 197 | PF00400 | 0.568 |
DEG_SPOP_SBC_1 | 134 | 138 | PF00917 | 0.547 |
DEG_SPOP_SBC_1 | 172 | 176 | PF00917 | 0.553 |
DOC_CKS1_1 | 191 | 196 | PF01111 | 0.650 |
DOC_MAPK_RevD_3 | 244 | 259 | PF00069 | 0.564 |
DOC_PP2B_LxvP_1 | 253 | 256 | PF13499 | 0.528 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.563 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.609 |
LIG_14-3-3_CanoR_1 | 108 | 113 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 123 | 130 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 286 | 295 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 79 | 87 | PF00244 | 0.602 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.654 |
LIG_BRCT_BRCA1_1 | 173 | 177 | PF00533 | 0.555 |
LIG_BRCT_BRCA1_1 | 198 | 202 | PF00533 | 0.679 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.649 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.527 |
LIG_FHA_2 | 191 | 197 | PF00498 | 0.647 |
LIG_FHA_2 | 209 | 215 | PF00498 | 0.629 |
LIG_LIR_Gen_1 | 27 | 36 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 251 | 257 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 27 | 31 | PF02991 | 0.674 |
LIG_MYND_1 | 215 | 219 | PF01753 | 0.672 |
LIG_SH2_PTP2 | 254 | 257 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.549 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.647 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.577 |
MOD_CDK_SPK_2 | 187 | 192 | PF00069 | 0.627 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.651 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.620 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.733 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.636 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.767 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.647 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.525 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.649 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.650 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.702 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.662 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.655 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.602 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.528 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.586 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.613 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.559 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.655 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.593 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.468 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.605 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.576 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.506 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.586 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.623 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.557 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.696 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.565 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.697 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.555 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.647 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.659 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.621 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.705 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.511 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.699 |
MOD_N-GLC_1 | 117 | 122 | PF02516 | 0.542 |
MOD_N-GLC_1 | 194 | 199 | PF02516 | 0.709 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.720 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.625 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.557 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.673 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.618 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.756 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.602 |
MOD_PIKK_1 | 123 | 129 | PF00454 | 0.610 |
MOD_PIKK_1 | 154 | 160 | PF00454 | 0.566 |
MOD_PKA_1 | 51 | 57 | PF00069 | 0.619 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.598 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.633 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.635 |
MOD_PKB_1 | 139 | 147 | PF00069 | 0.672 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.613 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.595 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.608 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.675 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.560 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.635 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.670 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.647 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.609 |
MOD_SUMO_rev_2 | 144 | 148 | PF00179 | 0.640 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.566 |
TRG_ER_diArg_1 | 257 | 259 | PF00400 | 0.548 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I411 | Leptomonas seymouri | 31% | 85% |
A4HMF7 | Leishmania braziliensis | 62% | 100% |
E9AEV8 | Leishmania major | 90% | 100% |
E9AHU5 | Leishmania infantum | 100% | 100% |
E9B614 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |