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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: A4HT79
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 67 | 71 | PF00656 | 0.560 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.524 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.507 |
CLV_PCSK_PC1ET2_1 | 112 | 114 | PF00082 | 0.516 |
CLV_PCSK_PC1ET2_1 | 99 | 101 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.487 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.440 |
DEG_SPOP_SBC_1 | 270 | 274 | PF00917 | 0.615 |
DOC_MAPK_FxFP_2 | 93 | 96 | PF00069 | 0.569 |
DOC_MAPK_gen_1 | 199 | 207 | PF00069 | 0.569 |
DOC_MAPK_gen_1 | 48 | 58 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 42 | 49 | PF00069 | 0.485 |
DOC_PP4_FxxP_1 | 93 | 96 | PF00568 | 0.457 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.724 |
DOC_USP7_UBL2_3 | 99 | 103 | PF12436 | 0.546 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.723 |
LIG_14-3-3_CanoR_1 | 121 | 127 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 187 | 193 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 261 | 267 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 269 | 276 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 42 | 46 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 61 | 69 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 76 | 84 | PF00244 | 0.332 |
LIG_BRCT_BRCA1_1 | 182 | 186 | PF00533 | 0.655 |
LIG_BRCT_BRCA1_1 | 224 | 228 | PF00533 | 0.693 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.614 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.444 |
LIG_FHA_2 | 65 | 71 | PF00498 | 0.564 |
LIG_LIR_Apic_2 | 91 | 97 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 265 | 271 | PF02991 | 0.657 |
LIG_LIR_Nem_3 | 70 | 75 | PF02991 | 0.456 |
LIG_Pex14_2 | 186 | 190 | PF04695 | 0.492 |
LIG_SH2_CRK | 268 | 272 | PF00017 | 0.618 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.504 |
MOD_CDC14_SPxK_1 | 137 | 140 | PF00782 | 0.784 |
MOD_CDK_SPxK_1 | 134 | 140 | PF00069 | 0.780 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.695 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.586 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.741 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.540 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.789 |
MOD_CK2_1 | 207 | 213 | PF00069 | 0.666 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.781 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.716 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.665 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.559 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.516 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.528 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.606 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.496 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.490 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.662 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.608 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.682 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.691 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.608 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.750 |
MOD_N-GLC_1 | 122 | 127 | PF02516 | 0.643 |
MOD_N-GLC_1 | 131 | 136 | PF02516 | 0.650 |
MOD_N-GLC_1 | 162 | 167 | PF02516 | 0.685 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.690 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.611 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.653 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.665 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.568 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.427 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.512 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.375 |
MOD_PIKK_1 | 140 | 146 | PF00454 | 0.706 |
MOD_PIKK_1 | 86 | 92 | PF00454 | 0.453 |
MOD_PK_1 | 212 | 218 | PF00069 | 0.705 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.635 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.765 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.435 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.438 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.646 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.652 |
MOD_Plk_1 | 28 | 34 | PF00069 | 0.557 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.673 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.724 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.720 |
MOD_SUMO_rev_2 | 191 | 201 | PF00179 | 0.552 |
TRG_ENDOCYTIC_2 | 268 | 271 | PF00928 | 0.621 |
TRG_ER_diArg_1 | 186 | 188 | PF00400 | 0.547 |
TRG_NES_CRM1_1 | 53 | 66 | PF08389 | 0.446 |
TRG_NLS_Bipartite_1 | 99 | 115 | PF00514 | 0.521 |
TRG_NLS_MonoExtC_3 | 110 | 115 | PF00514 | 0.565 |
TRG_Pf-PMV_PEXEL_1 | 103 | 107 | PF00026 | 0.574 |
TRG_Pf-PMV_PEXEL_1 | 61 | 66 | PF00026 | 0.555 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HSU4 | Leptomonas seymouri | 73% | 72% |
A0A1X0NPE0 | Trypanosomatidae | 47% | 74% |
A0A3S7WPV5 | Leishmania donovani | 100% | 71% |
A4H4Z9 | Leishmania braziliensis | 88% | 100% |
C9ZUQ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 78% |
E9AL61 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
Q4QIP3 | Leishmania major | 97% | 100% |
V5B859 | Trypanosoma cruzi | 44% | 87% |