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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A0A3Q8IG78
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 57 | 61 | PF00656 | 0.782 |
CLV_C14_Caspase3-7 | 8 | 12 | PF00656 | 0.686 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.513 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.506 |
CLV_PCSK_PC7_1 | 28 | 34 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.769 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.527 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.731 |
DOC_CKS1_1 | 172 | 177 | PF01111 | 0.774 |
DOC_CKS1_1 | 52 | 57 | PF01111 | 0.706 |
DOC_MAPK_MEF2A_6 | 256 | 264 | PF00069 | 0.504 |
DOC_PP2B_LxvP_1 | 135 | 138 | PF13499 | 0.810 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.792 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.762 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.771 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.809 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.750 |
LIG_14-3-3_CanoR_1 | 81 | 89 | PF00244 | 0.762 |
LIG_Actin_WH2_2 | 12 | 30 | PF00022 | 0.678 |
LIG_BIR_III_4 | 63 | 67 | PF00653 | 0.732 |
LIG_BIR_III_4 | 70 | 74 | PF00653 | 0.682 |
LIG_deltaCOP1_diTrp_1 | 97 | 108 | PF00928 | 0.694 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.773 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.686 |
LIG_FHA_2 | 316 | 322 | PF00498 | 0.430 |
LIG_LIR_Gen_1 | 149 | 160 | PF02991 | 0.675 |
LIG_LIR_Gen_1 | 174 | 180 | PF02991 | 0.749 |
LIG_LIR_Gen_1 | 21 | 31 | PF02991 | 0.685 |
LIG_LIR_Nem_3 | 149 | 155 | PF02991 | 0.677 |
LIG_LIR_Nem_3 | 174 | 179 | PF02991 | 0.745 |
LIG_LIR_Nem_3 | 21 | 27 | PF02991 | 0.677 |
LIG_LIR_Nem_3 | 77 | 82 | PF02991 | 0.702 |
LIG_NRBOX | 312 | 318 | PF00104 | 0.494 |
LIG_PDZ_Class_1 | 321 | 326 | PF00595 | 0.553 |
LIG_Pex14_1 | 108 | 112 | PF04695 | 0.683 |
LIG_Pex14_1 | 259 | 263 | PF04695 | 0.512 |
LIG_PTB_Apo_2 | 170 | 177 | PF02174 | 0.699 |
LIG_SH2_CRK | 156 | 160 | PF00017 | 0.689 |
LIG_SH2_CRK | 24 | 28 | PF00017 | 0.675 |
LIG_SH2_NCK_1 | 186 | 190 | PF00017 | 0.645 |
LIG_SH2_SRC | 186 | 189 | PF00017 | 0.704 |
LIG_SH2_STAP1 | 156 | 160 | PF00017 | 0.689 |
LIG_SH2_STAP1 | 294 | 298 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.638 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.686 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.702 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.769 |
MOD_CDC14_SPxK_1 | 225 | 228 | PF00782 | 0.788 |
MOD_CDK_SPxK_1 | 222 | 228 | PF00069 | 0.788 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.512 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.428 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.790 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.428 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.833 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.530 |
MOD_GlcNHglycan | 130 | 134 | PF01048 | 0.568 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.571 |
MOD_GlcNHglycan | 239 | 244 | PF01048 | 0.503 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.438 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.551 |
MOD_GlcNHglycan | 70 | 74 | PF01048 | 0.536 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.657 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.756 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.418 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.428 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.828 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.708 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.694 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.516 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.449 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.492 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.507 |
MOD_PIKK_1 | 117 | 123 | PF00454 | 0.717 |
MOD_PIKK_1 | 201 | 207 | PF00454 | 0.799 |
MOD_PIKK_1 | 305 | 311 | PF00454 | 0.494 |
MOD_PKA_1 | 93 | 99 | PF00069 | 0.767 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.767 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.663 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.776 |
MOD_Plk_1 | 320 | 326 | PF00069 | 0.435 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.677 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.572 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.771 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.757 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.810 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.750 |
TRG_DiLeu_BaEn_1 | 22 | 27 | PF01217 | 0.675 |
TRG_DiLeu_BaEn_4 | 97 | 103 | PF01217 | 0.765 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.690 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.686 |
TRG_ER_diArg_1 | 249 | 252 | PF00400 | 0.714 |
TRG_ER_diArg_1 | 31 | 33 | PF00400 | 0.693 |
TRG_ER_diArg_1 | 87 | 90 | PF00400 | 0.731 |
TRG_NES_CRM1_1 | 8 | 22 | PF08389 | 0.680 |
TRG_Pf-PMV_PEXEL_1 | 228 | 232 | PF00026 | 0.559 |
TRG_Pf-PMV_PEXEL_1 | 81 | 85 | PF00026 | 0.565 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9K1 | Leptomonas seymouri | 41% | 98% |
A4HML3 | Leishmania braziliensis | 70% | 99% |
A4IB90 | Leishmania infantum | 99% | 100% |
E9AF14 | Leishmania major | 90% | 100% |
E9B670 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |