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: 1, no: 9 |
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: Q4Q9E7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.488 |
CLV_PCSK_FUR_1 | 25 | 29 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.316 |
DOC_CYCLIN_RxL_1 | 218 | 230 | PF00134 | 0.602 |
DOC_MAPK_gen_1 | 22 | 31 | PF00069 | 0.680 |
DOC_MAPK_MEF2A_6 | 25 | 33 | PF00069 | 0.655 |
DOC_PP1_RVXF_1 | 222 | 229 | PF00149 | 0.474 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.789 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.764 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.716 |
LIG_14-3-3_CanoR_1 | 164 | 174 | PF00244 | 0.710 |
LIG_14-3-3_CanoR_1 | 27 | 32 | PF00244 | 0.716 |
LIG_14-3-3_CanoR_1 | 92 | 102 | PF00244 | 0.694 |
LIG_BRCT_BRCA1_1 | 45 | 49 | PF00533 | 0.713 |
LIG_BRCT_BRCA1_1 | 96 | 100 | PF00533 | 0.686 |
LIG_deltaCOP1_diTrp_1 | 301 | 310 | PF00928 | 0.454 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.739 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.729 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.664 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.794 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.781 |
LIG_LIR_Gen_1 | 230 | 239 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 308 | 316 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 230 | 235 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 300 | 306 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 308 | 313 | PF02991 | 0.386 |
LIG_PCNA_PIPBox_1 | 182 | 191 | PF02747 | 0.677 |
LIG_Pex14_1 | 228 | 232 | PF04695 | 0.335 |
LIG_SH2_CRK | 223 | 227 | PF00017 | 0.502 |
LIG_SH2_CRK | 250 | 254 | PF00017 | 0.415 |
LIG_SH2_STAP1 | 20 | 24 | PF00017 | 0.591 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.627 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.444 |
LIG_SH3_2 | 211 | 216 | PF14604 | 0.566 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.734 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.713 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.453 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.693 |
LIG_SH3_3 | 38 | 44 | PF00018 | 0.739 |
LIG_SUMO_SIM_anti_2 | 30 | 35 | PF11976 | 0.602 |
LIG_SUMO_SIM_par_1 | 292 | 297 | PF11976 | 0.426 |
LIG_TRAF2_1 | 124 | 127 | PF00917 | 0.696 |
LIG_TRAF2_1 | 317 | 320 | PF00917 | 0.379 |
LIG_TYR_ITIM | 221 | 226 | PF00017 | 0.611 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.751 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.786 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.761 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.724 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.626 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.616 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.776 |
MOD_CK2_1 | 314 | 320 | PF00069 | 0.412 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.425 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.479 |
MOD_GlcNHglycan | 159 | 163 | PF01048 | 0.488 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.568 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.538 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.646 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.539 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.788 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.723 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.638 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.675 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.651 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.336 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.337 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.748 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.731 |
MOD_NEK2_2 | 249 | 254 | PF00069 | 0.472 |
MOD_NEK2_2 | 285 | 290 | PF00069 | 0.371 |
MOD_PIKK_1 | 95 | 101 | PF00454 | 0.708 |
MOD_PK_1 | 27 | 33 | PF00069 | 0.779 |
MOD_PKA_1 | 27 | 33 | PF00069 | 0.753 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.685 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.753 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.495 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.695 |
MOD_PKB_1 | 25 | 33 | PF00069 | 0.602 |
MOD_Plk_1 | 138 | 144 | PF00069 | 0.578 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.737 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.723 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.758 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.767 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.715 |
TRG_ENDOCYTIC_2 | 223 | 226 | PF00928 | 0.561 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.410 |
TRG_ER_diArg_1 | 24 | 27 | PF00400 | 0.691 |
TRG_Pf-PMV_PEXEL_1 | 254 | 258 | PF00026 | 0.665 |
TRG_Pf-PMV_PEXEL_1 | 304 | 308 | PF00026 | 0.602 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P498 | Leptomonas seymouri | 47% | 100% |
A0A1X0NSG9 | Trypanosomatidae | 33% | 100% |
A0A3R7MX83 | Trypanosoma rangeli | 30% | 100% |
A0A3S7WZN6 | Leishmania donovani | 88% | 100% |
A4HEQ0 | Leishmania braziliensis | 61% | 100% |
A4I1Y0 | Leishmania infantum | 88% | 100% |
C9ZS39 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AY26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
V5B9G1 | Trypanosoma cruzi | 36% | 100% |