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. | yes | yes: 10 |
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 | yes | yes: 5, no: 1 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4HWF5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 123 | 127 | PF00656 | 0.537 |
CLV_C14_Caspase3-7 | 273 | 277 | PF00656 | 0.509 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.670 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.669 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.688 |
DEG_ODPH_VHL_1 | 15 | 26 | PF01847 | 0.493 |
DEG_SPOP_SBC_1 | 108 | 112 | PF00917 | 0.473 |
DEG_SPOP_SBC_1 | 137 | 141 | PF00917 | 0.578 |
DOC_CDC14_PxL_1 | 13 | 21 | PF14671 | 0.519 |
DOC_CYCLIN_yCln2_LP_2 | 9 | 15 | PF00134 | 0.537 |
DOC_MAPK_gen_1 | 230 | 240 | PF00069 | 0.412 |
DOC_PP1_RVXF_1 | 284 | 290 | PF00149 | 0.396 |
DOC_PP2B_LxvP_1 | 241 | 244 | PF13499 | 0.414 |
DOC_PP2B_LxvP_1 | 9 | 12 | PF13499 | 0.541 |
DOC_PP4_MxPP_1 | 182 | 185 | PF00568 | 0.409 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.377 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.447 |
DOC_USP7_UBL2_3 | 75 | 79 | PF12436 | 0.448 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.536 |
LIG_14-3-3_CanoR_1 | 31 | 39 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 316 | 321 | PF00244 | 0.351 |
LIG_APCC_ABBA_1 | 196 | 201 | PF00400 | 0.504 |
LIG_BRCT_BRCA1_1 | 117 | 121 | PF00533 | 0.529 |
LIG_Clathr_ClatBox_1 | 297 | 301 | PF01394 | 0.414 |
LIG_CSL_BTD_1 | 119 | 122 | PF09270 | 0.526 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.495 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.544 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.430 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.447 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.529 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.503 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.470 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.435 |
LIG_Integrin_isoDGR_2 | 264 | 266 | PF01839 | 0.659 |
LIG_MYND_1 | 181 | 185 | PF01753 | 0.476 |
LIG_NRBOX | 19 | 25 | PF00104 | 0.490 |
LIG_PCNA_yPIPBox_3 | 188 | 199 | PF02747 | 0.476 |
LIG_SH2_CRK | 205 | 209 | PF00017 | 0.446 |
LIG_SH2_GRB2like | 205 | 208 | PF00017 | 0.445 |
LIG_SH2_NCK_1 | 106 | 110 | PF00017 | 0.436 |
LIG_SH2_NCK_1 | 199 | 203 | PF00017 | 0.491 |
LIG_SH2_NCK_1 | 205 | 209 | PF00017 | 0.558 |
LIG_SH2_SRC | 205 | 208 | PF00017 | 0.434 |
LIG_SH2_SRC | 52 | 55 | PF00017 | 0.400 |
LIG_SH2_STAP1 | 199 | 203 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 52 | 56 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.429 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.527 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.541 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.419 |
LIG_SH3_3 | 304 | 310 | PF00018 | 0.501 |
LIG_SUMO_SIM_anti_2 | 22 | 27 | PF11976 | 0.525 |
LIG_SUMO_SIM_par_1 | 16 | 22 | PF11976 | 0.511 |
LIG_TRAF2_1 | 153 | 156 | PF00917 | 0.536 |
LIG_TRFH_1 | 298 | 302 | PF08558 | 0.418 |
MOD_CDK_SPK_2 | 225 | 230 | PF00069 | 0.411 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.444 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.456 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.497 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.535 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.516 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.508 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.508 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.795 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.704 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.677 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.761 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.632 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.681 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.662 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.549 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.494 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.506 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.507 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.518 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.419 |
MOD_N-GLC_1 | 104 | 109 | PF02516 | 0.679 |
MOD_N-GLC_1 | 221 | 226 | PF02516 | 0.720 |
MOD_N-GLC_2 | 260 | 262 | PF02516 | 0.603 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.390 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.523 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.449 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.516 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.608 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.422 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.494 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.544 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.446 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.484 |
MOD_Plk_1 | 90 | 96 | PF00069 | 0.428 |
MOD_Plk_2-3 | 151 | 157 | PF00069 | 0.515 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.599 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.497 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.332 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.509 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.404 |
MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.538 |
TRG_DiLeu_BaLyEn_6 | 14 | 19 | PF01217 | 0.571 |
TRG_DiLeu_BaLyEn_6 | 313 | 318 | PF01217 | 0.304 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.451 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P748 | Leptomonas seymouri | 39% | 100% |
A0A3S7WTK4 | Leishmania donovani | 99% | 100% |
A4H829 | Leishmania braziliensis | 64% | 100% |
E9AQ54 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4QFC8 | Leishmania major | 89% | 100% |