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: Q4Q4G8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.453 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.450 |
CLV_PCSK_PC1ET2_1 | 239 | 241 | PF00082 | 0.502 |
CLV_PCSK_PC1ET2_1 | 354 | 356 | PF00082 | 0.426 |
CLV_PCSK_PC1ET2_1 | 39 | 41 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.451 |
DEG_APCC_DBOX_1 | 130 | 138 | PF00400 | 0.456 |
DEG_ODPH_VHL_1 | 272 | 284 | PF01847 | 0.424 |
DEG_SPOP_SBC_1 | 62 | 66 | PF00917 | 0.607 |
DOC_CYCLIN_yCln2_LP_2 | 241 | 247 | PF00134 | 0.499 |
DOC_CYCLIN_yCln2_LP_2 | 54 | 60 | PF00134 | 0.531 |
DOC_MAPK_gen_1 | 39 | 48 | PF00069 | 0.506 |
DOC_MAPK_MEF2A_6 | 29 | 37 | PF00069 | 0.498 |
DOC_PP2B_LxvP_1 | 253 | 256 | PF13499 | 0.445 |
DOC_PP2B_LxvP_1 | 54 | 57 | PF13499 | 0.545 |
DOC_PP4_FxxP_1 | 347 | 350 | PF00568 | 0.337 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.607 |
DOC_USP7_UBL2_3 | 239 | 243 | PF12436 | 0.500 |
DOC_USP7_UBL2_3 | 299 | 303 | PF12436 | 0.400 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.632 |
LIG_14-3-3_CanoR_1 | 102 | 108 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 129 | 138 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 141 | 149 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 204 | 209 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 233 | 241 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 302 | 312 | PF00244 | 0.338 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.606 |
LIG_eIF4E_1 | 21 | 27 | PF01652 | 0.465 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.472 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.362 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.469 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.586 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.548 |
LIG_FHA_2 | 130 | 136 | PF00498 | 0.530 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.536 |
LIG_FHA_2 | 284 | 290 | PF00498 | 0.365 |
LIG_IRF3_LxIS_1 | 185 | 192 | PF10401 | 0.581 |
LIG_LIR_Apic_2 | 346 | 350 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 28 | 37 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 331 | 340 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 28 | 33 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 331 | 337 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 42 | 48 | PF02991 | 0.445 |
LIG_Pex14_2 | 347 | 351 | PF04695 | 0.338 |
LIG_REV1ctd_RIR_1 | 293 | 303 | PF16727 | 0.273 |
LIG_SH2_CRK | 269 | 273 | PF00017 | 0.353 |
LIG_SH2_CRK | 30 | 34 | PF00017 | 0.419 |
LIG_SH2_CRK | 58 | 62 | PF00017 | 0.544 |
LIG_SH2_GRB2like | 311 | 314 | PF00017 | 0.356 |
LIG_SH2_NCK_1 | 222 | 226 | PF00017 | 0.536 |
LIG_SH2_SRC | 21 | 24 | PF00017 | 0.497 |
LIG_SH2_STAP1 | 17 | 21 | PF00017 | 0.499 |
LIG_SH2_STAP1 | 222 | 226 | PF00017 | 0.536 |
LIG_SH2_STAP1 | 58 | 62 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.330 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.539 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.499 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.429 |
LIG_SH3_3 | 353 | 359 | PF00018 | 0.477 |
LIG_SUMO_SIM_par_1 | 280 | 286 | PF11976 | 0.426 |
LIG_TYR_ITIM | 56 | 61 | PF00017 | 0.559 |
LIG_UBA3_1 | 308 | 317 | PF00899 | 0.423 |
LIG_WRC_WIRS_1 | 344 | 349 | PF05994 | 0.323 |
MOD_CDC14_SPxK_1 | 95 | 98 | PF00782 | 0.595 |
MOD_CDK_SPK_2 | 86 | 91 | PF00069 | 0.607 |
MOD_CDK_SPxK_1 | 92 | 98 | PF00069 | 0.602 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.579 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.664 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.553 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.615 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.563 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.551 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.372 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.385 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.571 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.628 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.622 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.514 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.650 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.727 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.598 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.517 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.516 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.640 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.548 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.661 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.580 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.590 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.446 |
MOD_N-GLC_1 | 72 | 77 | PF02516 | 0.509 |
MOD_N-GLC_2 | 124 | 126 | PF02516 | 0.586 |
MOD_N-GLC_2 | 313 | 315 | PF02516 | 0.378 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.656 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.574 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.465 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.392 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.432 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.486 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.530 |
MOD_NEK2_2 | 9 | 14 | PF00069 | 0.540 |
MOD_PIKK_1 | 46 | 52 | PF00454 | 0.500 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.623 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.533 |
MOD_PKB_1 | 202 | 210 | PF00069 | 0.496 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.427 |
MOD_Plk_2-3 | 335 | 341 | PF00069 | 0.402 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.524 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.506 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.551 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.627 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.546 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.590 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.622 |
MOD_SUMO_rev_2 | 232 | 241 | PF00179 | 0.466 |
TRG_ENDOCYTIC_2 | 10 | 13 | PF00928 | 0.597 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 30 | 33 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.566 |
TRG_ER_diArg_1 | 128 | 131 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 140 | 143 | PF00400 | 0.550 |
TRG_ER_diArg_1 | 196 | 199 | PF00400 | 0.695 |
TRG_NLS_MonoExtN_4 | 350 | 357 | PF00514 | 0.405 |
TRG_Pf-PMV_PEXEL_1 | 233 | 237 | PF00026 | 0.533 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P717 | Leptomonas seymouri | 50% | 100% |
A0A3Q8IJX1 | Leishmania donovani | 90% | 100% |
A4HL74 | Leishmania braziliensis | 65% | 100% |
A4I8Q3 | Leishmania infantum | 90% | 100% |
E9B3L7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |