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: 10 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005743 | mitochondrial inner membrane | 5 | 1 |
GO:0019866 | organelle inner membrane | 4 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031966 | mitochondrial membrane | 4 | 1 |
Related structures:
AlphaFold database: E9AY26
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.467 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.644 |
DOC_PP4_FxxP_1 | 190 | 193 | PF00568 | 0.661 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.691 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.644 |
LIG_14-3-3_CanoR_1 | 16 | 24 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 27 | 32 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 92 | 102 | PF00244 | 0.671 |
LIG_BRCT_BRCA1_1 | 45 | 49 | PF00533 | 0.712 |
LIG_BRCT_BRCA1_1 | 96 | 100 | PF00533 | 0.700 |
LIG_deltaCOP1_diTrp_1 | 302 | 311 | PF00928 | 0.434 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.735 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.298 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.665 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.665 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.689 |
LIG_FHA_2 | 71 | 77 | PF00498 | 0.606 |
LIG_LIR_Gen_1 | 230 | 239 | PF02991 | 0.275 |
LIG_LIR_Gen_1 | 309 | 318 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 230 | 235 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 301 | 307 | PF02991 | 0.378 |
LIG_PCNA_PIPBox_1 | 182 | 191 | PF02747 | 0.614 |
LIG_Pex14_1 | 228 | 232 | PF04695 | 0.275 |
LIG_SH2_CRK | 223 | 227 | PF00017 | 0.507 |
LIG_SH2_CRK | 250 | 254 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.413 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.642 |
LIG_SH3_3 | 294 | 300 | PF00018 | 0.377 |
LIG_SH3_3 | 38 | 44 | PF00018 | 0.706 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.535 |
LIG_SUMO_SIM_par_1 | 293 | 298 | PF11976 | 0.371 |
LIG_TRAF2_1 | 124 | 127 | PF00917 | 0.680 |
LIG_TRAF2_1 | 318 | 321 | PF00917 | 0.359 |
LIG_TRFH_1 | 100 | 104 | PF08558 | 0.570 |
LIG_TYR_ITIM | 221 | 226 | PF00017 | 0.610 |
MOD_CDK_SPK_2 | 189 | 194 | PF00069 | 0.536 |
MOD_CDK_SPK_2 | 211 | 216 | PF00069 | 0.530 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.693 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.723 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.656 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.688 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.608 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.615 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.763 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.522 |
MOD_CK2_1 | 262 | 268 | PF00069 | 0.336 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.612 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.462 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.466 |
MOD_GlcNHglycan | 159 | 163 | PF01048 | 0.450 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.514 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.619 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.527 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.765 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.463 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.672 |
MOD_LATS_1 | 25 | 31 | PF00433 | 0.653 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.599 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.302 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.202 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.627 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.731 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.736 |
MOD_NEK2_2 | 249 | 254 | PF00069 | 0.381 |
MOD_NEK2_2 | 87 | 92 | PF00069 | 0.570 |
MOD_PIKK_1 | 206 | 212 | PF00454 | 0.732 |
MOD_PIKK_1 | 33 | 39 | PF00454 | 0.766 |
MOD_PK_1 | 27 | 33 | PF00069 | 0.684 |
MOD_PKA_1 | 16 | 22 | PF00069 | 0.568 |
MOD_PKA_1 | 27 | 33 | PF00069 | 0.731 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.574 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.568 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.731 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.650 |
MOD_Plk_1 | 138 | 144 | PF00069 | 0.545 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.633 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.475 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.754 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.704 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.699 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.747 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.637 |
MOD_SUMO_for_1 | 193 | 196 | PF00179 | 0.584 |
TRG_ENDOCYTIC_2 | 223 | 226 | PF00928 | 0.585 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.433 |
TRG_ER_diArg_1 | 15 | 17 | PF00400 | 0.658 |
TRG_ER_diArg_1 | 26 | 28 | PF00400 | 0.650 |
TRG_Pf-PMV_PEXEL_1 | 254 | 258 | PF00026 | 0.636 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P498 | Leptomonas seymouri | 49% | 100% |
A0A0S4KLN6 | Bodo saltans | 29% | 100% |
A0A1X0NSG9 | Trypanosomatidae | 36% | 100% |
A0A3R7MX83 | Trypanosoma rangeli | 34% | 100% |
A0A3S7WZN6 | Leishmania donovani | 82% | 100% |
A4HEQ0 | Leishmania braziliensis | 61% | 100% |
A4I1Y0 | Leishmania infantum | 82% | 100% |
C9ZS39 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
Q4Q9E7 | Leishmania major | 86% | 100% |
V5B9G1 | Trypanosoma cruzi | 36% | 100% |