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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: Q4QDP2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.387 |
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.292 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.479 |
CLV_PCSK_FUR_1 | 315 | 319 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 317 | 319 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.479 |
CLV_PCSK_PC1ET2_1 | 314 | 316 | PF00082 | 0.375 |
CLV_PCSK_PC7_1 | 313 | 319 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.403 |
DOC_CDC14_PxL_1 | 80 | 88 | PF14671 | 0.667 |
DOC_MAPK_MEF2A_6 | 104 | 111 | PF00069 | 0.607 |
DOC_PP4_FxxP_1 | 132 | 135 | PF00568 | 0.611 |
DOC_PP4_FxxP_1 | 196 | 199 | PF00568 | 0.657 |
DOC_PP4_FxxP_1 | 232 | 235 | PF00568 | 0.587 |
DOC_PP4_FxxP_1 | 261 | 264 | PF00568 | 0.528 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.797 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.778 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.459 |
DOC_USP7_MATH_2 | 190 | 196 | PF00917 | 0.755 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.633 |
LIG_14-3-3_CanoR_1 | 64 | 73 | PF00244 | 0.779 |
LIG_14-3-3_CanoR_1 | 85 | 91 | PF00244 | 0.620 |
LIG_APCC_ABBA_1 | 270 | 275 | PF00400 | 0.540 |
LIG_BRCT_BRCA1_1 | 228 | 232 | PF00533 | 0.600 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.588 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.677 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.569 |
LIG_LIR_Apic_2 | 194 | 199 | PF02991 | 0.651 |
LIG_LIR_Apic_2 | 229 | 235 | PF02991 | 0.595 |
LIG_LIR_Apic_2 | 260 | 264 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 220 | 225 | PF02991 | 0.668 |
LIG_LIR_Gen_1 | 279 | 290 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 114 | 118 | PF02991 | 0.629 |
LIG_LIR_Nem_3 | 136 | 141 | PF02991 | 0.665 |
LIG_LIR_Nem_3 | 194 | 200 | PF02991 | 0.651 |
LIG_LIR_Nem_3 | 220 | 224 | PF02991 | 0.669 |
LIG_LIR_Nem_3 | 255 | 261 | PF02991 | 0.614 |
LIG_LIR_Nem_3 | 279 | 285 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 329 | 334 | PF02991 | 0.414 |
LIG_PCNA_yPIPBox_3 | 284 | 295 | PF02747 | 0.556 |
LIG_Pex14_1 | 331 | 335 | PF04695 | 0.480 |
LIG_Pex14_2 | 196 | 200 | PF04695 | 0.652 |
LIG_Pex14_2 | 261 | 265 | PF04695 | 0.531 |
LIG_REV1ctd_RIR_1 | 135 | 143 | PF16727 | 0.668 |
LIG_SH2_CRK | 164 | 168 | PF00017 | 0.708 |
LIG_SH2_SRC | 321 | 324 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 164 | 168 | PF00017 | 0.699 |
LIG_SH2_STAT5 | 321 | 324 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.647 |
LIG_SH3_3 | 13 | 19 | PF00018 | 0.713 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.763 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.594 |
LIG_SUMO_SIM_anti_2 | 123 | 128 | PF11976 | 0.561 |
LIG_SUMO_SIM_anti_2 | 289 | 294 | PF11976 | 0.579 |
LIG_TYR_ITIM | 333 | 338 | PF00017 | 0.480 |
LIG_WRC_WIRS_1 | 193 | 198 | PF05994 | 0.749 |
LIG_WRC_WIRS_1 | 237 | 242 | PF05994 | 0.613 |
LIG_WRC_WIRS_1 | 258 | 263 | PF05994 | 0.544 |
LIG_WW_3 | 168 | 172 | PF00397 | 0.691 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.736 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.728 |
MOD_CK2_1 | 298 | 304 | PF00069 | 0.591 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.554 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.523 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.714 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.571 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.580 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.524 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.642 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.754 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.599 |
MOD_N-GLC_1 | 208 | 213 | PF02516 | 0.473 |
MOD_N-GLC_1 | 293 | 298 | PF02516 | 0.472 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.664 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.631 |
MOD_NEK2_2 | 226 | 231 | PF00069 | 0.626 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.590 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.758 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.639 |
MOD_Plk_1 | 120 | 126 | PF00069 | 0.611 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.674 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.603 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.678 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.741 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.571 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.558 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.407 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.673 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.635 |
TRG_ENDOCYTIC_2 | 115 | 118 | PF00928 | 0.522 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.714 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.644 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.562 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.560 |
TRG_ER_diArg_1 | 315 | 318 | PF00400 | 0.634 |
TRG_ER_diArg_1 | 32 | 34 | PF00400 | 0.766 |
TRG_ER_diArg_1 | 84 | 87 | PF00400 | 0.594 |
TRG_NLS_MonoExtC_3 | 312 | 317 | PF00514 | 0.600 |
TRG_NLS_MonoExtN_4 | 313 | 318 | PF00514 | 0.601 |
TRG_Pf-PMV_PEXEL_1 | 116 | 121 | PF00026 | 0.289 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HX40 | Leptomonas seymouri | 75% | 97% |
A0A0S4JJX8 | Bodo saltans | 52% | 100% |
A0A1X0P7D7 | Trypanosomatidae | 63% | 100% |
A0A3S7WV34 | Leishmania donovani | 94% | 100% |
A4H9Q0 | Leishmania braziliensis | 78% | 100% |
A4HY17 | Leishmania infantum | 94% | 100% |
D0A568 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
E9ART1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5BJ52 | Trypanosoma cruzi | 60% | 100% |