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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QBC8
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0016874 | ligase activity | 2 | 7 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 7 |
GO:0016880 | acid-ammonia (or amide) ligase activity | 4 | 7 |
GO:0047479 | trypanothione synthase activity | 5 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.440 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.440 |
CLV_PCSK_PC1ET2_1 | 136 | 138 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.456 |
DEG_MDM2_SWIB_1 | 121 | 128 | PF02201 | 0.320 |
DEG_SPOP_SBC_1 | 67 | 71 | PF00917 | 0.664 |
DOC_CKS1_1 | 26 | 31 | PF01111 | 0.621 |
DOC_CYCLIN_RxL_1 | 128 | 138 | PF00134 | 0.253 |
DOC_CYCLIN_yCln2_LP_2 | 216 | 219 | PF00134 | 0.239 |
DOC_PP2B_LxvP_1 | 132 | 135 | PF13499 | 0.240 |
DOC_PP2B_LxvP_1 | 216 | 219 | PF13499 | 0.239 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.239 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.288 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.162 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.582 |
DOC_USP7_UBL2_3 | 205 | 209 | PF12436 | 0.292 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.275 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.331 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.617 |
LIG_14-3-3_CanoR_1 | 23 | 29 | PF00244 | 0.706 |
LIG_14-3-3_CanoR_1 | 68 | 76 | PF00244 | 0.515 |
LIG_deltaCOP1_diTrp_1 | 201 | 210 | PF00928 | 0.320 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.348 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.239 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.334 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.632 |
LIG_LIR_Apic_2 | 230 | 234 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 201 | 211 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 108 | 114 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 201 | 206 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 233 | 238 | PF02991 | 0.298 |
LIG_Pex14_1 | 102 | 106 | PF04695 | 0.306 |
LIG_Pex14_2 | 121 | 125 | PF04695 | 0.240 |
LIG_RPA_C_Fungi | 63 | 75 | PF08784 | 0.435 |
LIG_SH2_GRB2like | 92 | 95 | PF00017 | 0.371 |
LIG_SH2_STAP1 | 148 | 152 | PF00017 | 0.409 |
LIG_SH2_STAT3 | 114 | 117 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 84 | 87 | PF00017 | 0.501 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.664 |
LIG_TRAF2_1 | 43 | 46 | PF00917 | 0.576 |
MOD_CDK_SPxxK_3 | 13 | 20 | PF00069 | 0.524 |
MOD_CDK_SPxxK_3 | 25 | 32 | PF00069 | 0.479 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.324 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.492 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.361 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.473 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.667 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.414 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.663 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.427 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.401 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.606 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.596 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.567 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.233 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.418 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.468 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.686 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.660 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.496 |
MOD_N-GLC_1 | 93 | 98 | PF02516 | 0.432 |
MOD_N-GLC_2 | 105 | 107 | PF02516 | 0.273 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.423 |
MOD_NEK2_2 | 74 | 79 | PF00069 | 0.528 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.602 |
MOD_OFUCOSY | 139 | 146 | PF10250 | 0.409 |
MOD_PIKK_1 | 157 | 163 | PF00454 | 0.299 |
MOD_PKA_1 | 153 | 159 | PF00069 | 0.212 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.723 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.212 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.663 |
MOD_Plk_1 | 154 | 160 | PF00069 | 0.212 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.227 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.325 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.271 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.564 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.710 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.324 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.404 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.549 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.615 |
MOD_SPalmitoyl_4 | 1 | 7 | PF01529 | 0.540 |
MOD_SUMO_rev_2 | 5 | 12 | PF00179 | 0.603 |
TRG_DiLeu_BaLyEn_6 | 128 | 133 | PF01217 | 0.409 |
TRG_ER_diArg_1 | 123 | 125 | PF00400 | 0.277 |
TRG_ER_diArg_1 | 248 | 251 | PF00400 | 0.212 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1II02 | Leptomonas seymouri | 55% | 100% |
A0A0S4IVA9 | Bodo saltans | 35% | 87% |
A0A3S7WXK4 | Leishmania donovani | 84% | 82% |
A0A422N6B5 | Trypanosoma rangeli | 36% | 100% |
A4HCR0 | Leishmania braziliensis | 69% | 100% |
A4I085 | Leishmania infantum | 84% | 82% |
C9ZV01 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AW49 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 89% |
V5BCE6 | Trypanosoma cruzi | 36% | 93% |