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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4IAN9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 271 | 275 | PF00656 | 0.571 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 266 | 268 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.446 |
CLV_PCSK_FUR_1 | 243 | 247 | PF00082 | 0.595 |
CLV_PCSK_FUR_1 | 260 | 264 | PF00082 | 0.465 |
CLV_PCSK_FUR_1 | 73 | 77 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.446 |
CLV_PCSK_PC1ET2_1 | 244 | 246 | PF00082 | 0.565 |
CLV_PCSK_PC1ET2_1 | 75 | 77 | PF00082 | 0.566 |
CLV_PCSK_PC1ET2_1 | 92 | 94 | PF00082 | 0.268 |
CLV_PCSK_PC7_1 | 241 | 247 | PF00082 | 0.407 |
CLV_PCSK_PC7_1 | 258 | 264 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 76 | 80 | PF00082 | 0.585 |
DEG_APCC_DBOX_1 | 250 | 258 | PF00400 | 0.602 |
DEG_COP1_1 | 183 | 192 | PF00400 | 0.562 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.631 |
DOC_USP7_UBL2_3 | 75 | 79 | PF12436 | 0.614 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.600 |
LIG_14-3-3_CanoR_1 | 109 | 115 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 262 | 266 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 48 | 55 | PF00244 | 0.433 |
LIG_BRCT_BRCA1_1 | 58 | 62 | PF00533 | 0.568 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.412 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.535 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.534 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.617 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.638 |
LIG_LIR_Gen_1 | 213 | 222 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 66 | 74 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 132 | 136 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 213 | 218 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 66 | 70 | PF02991 | 0.646 |
LIG_OCRL_FandH_1 | 21 | 33 | PF00620 | 0.421 |
LIG_PDZ_Class_3 | 277 | 282 | PF00595 | 0.639 |
LIG_Pex14_1 | 129 | 133 | PF04695 | 0.328 |
LIG_Pex14_1 | 58 | 62 | PF04695 | 0.533 |
LIG_Pex14_2 | 63 | 67 | PF04695 | 0.522 |
LIG_SH2_CRK | 157 | 161 | PF00017 | 0.449 |
LIG_SH2_GRB2like | 89 | 92 | PF00017 | 0.385 |
LIG_SH2_STAT3 | 136 | 139 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.599 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.569 |
LIG_TRAF2_1 | 137 | 140 | PF00917 | 0.449 |
LIG_TRAF2_1 | 194 | 197 | PF00917 | 0.729 |
LIG_TRAF2_1 | 222 | 225 | PF00917 | 0.480 |
LIG_WRC_WIRS_1 | 67 | 72 | PF05994 | 0.556 |
MOD_CDK_SPxxK_3 | 195 | 202 | PF00069 | 0.528 |
MOD_CDK_SPxxK_3 | 79 | 86 | PF00069 | 0.602 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.440 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.657 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.620 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.531 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.420 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.564 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.665 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.633 |
MOD_CMANNOS | 55 | 58 | PF00535 | 0.542 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.717 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.507 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.435 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.465 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.619 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.707 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.576 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.425 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.509 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.647 |
MOD_N-GLC_1 | 79 | 84 | PF02516 | 0.614 |
MOD_N-GLC_2 | 146 | 148 | PF02516 | 0.328 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.421 |
MOD_NEK2_2 | 58 | 63 | PF00069 | 0.532 |
MOD_PIKK_1 | 135 | 141 | PF00454 | 0.447 |
MOD_PIKK_1 | 268 | 274 | PF00454 | 0.556 |
MOD_PIKK_1 | 36 | 42 | PF00454 | 0.431 |
MOD_PK_1 | 56 | 62 | PF00069 | 0.432 |
MOD_PKA_1 | 267 | 273 | PF00069 | 0.636 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.437 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.521 |
MOD_PKA_2 | 250 | 256 | PF00069 | 0.628 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.302 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.528 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.530 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.601 |
TRG_DiLeu_BaEn_4 | 225 | 231 | PF01217 | 0.490 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.433 |
TRG_ER_diArg_1 | 242 | 245 | PF00400 | 0.600 |
TRG_Pf-PMV_PEXEL_1 | 16 | 20 | PF00026 | 0.401 |
TRG_Pf-PMV_PEXEL_1 | 236 | 240 | PF00026 | 0.462 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAJ2 | Leptomonas seymouri | 63% | 100% |
A0A0S4KI64 | Bodo saltans | 40% | 100% |
A0A1X0PAK0 | Trypanosomatidae | 40% | 100% |
A0A3S7X7J4 | Leishmania donovani | 100% | 100% |
A0A422MR74 | Trypanosoma rangeli | 42% | 100% |
A4HAH9 | Leishmania braziliensis | 77% | 100% |
C9ZN14 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 98% |
E9B4N9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4Q3D7 | Leishmania major | 91% | 100% |
V5BJE2 | Trypanosoma cruzi | 40% | 96% |