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:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7X6L8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 60 | 64 | PF00656 | 0.668 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.685 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.632 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.596 |
CLV_PCSK_PC1ET2_1 | 95 | 97 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.659 |
DOC_CKS1_1 | 82 | 87 | PF01111 | 0.641 |
DOC_CYCLIN_RxL_1 | 208 | 216 | PF00134 | 0.646 |
DOC_CYCLIN_yClb3_PxF_3 | 149 | 157 | PF00134 | 0.721 |
DOC_PP1_RVXF_1 | 93 | 100 | PF00149 | 0.607 |
DOC_PP2B_LxvP_1 | 261 | 264 | PF13499 | 0.692 |
DOC_PP4_FxxP_1 | 118 | 121 | PF00568 | 0.614 |
DOC_PP4_FxxP_1 | 246 | 249 | PF00568 | 0.683 |
DOC_PP4_FxxP_1 | 257 | 260 | PF00568 | 0.601 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.665 |
DOC_USP7_MATH_2 | 88 | 94 | PF00917 | 0.613 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.679 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.797 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.720 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.575 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.625 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.633 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.689 |
LIG_FHA_2 | 188 | 194 | PF00498 | 0.676 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.600 |
LIG_LIR_Apic_2 | 116 | 121 | PF02991 | 0.610 |
LIG_LIR_Apic_2 | 243 | 249 | PF02991 | 0.641 |
LIG_LIR_Apic_2 | 254 | 260 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 212 | 217 | PF02991 | 0.653 |
LIG_PDZ_Class_2 | 260 | 265 | PF00595 | 0.595 |
LIG_Pex14_2 | 214 | 218 | PF04695 | 0.697 |
LIG_Pex14_2 | 246 | 250 | PF04695 | 0.628 |
LIG_SH2_NCK_1 | 130 | 134 | PF00017 | 0.806 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.723 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.743 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.696 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.657 |
LIG_SUMO_SIM_par_1 | 9 | 17 | PF11976 | 0.801 |
LIG_TRAF2_1 | 2 | 5 | PF00917 | 0.776 |
LIG_TRAF2_1 | 58 | 61 | PF00917 | 0.633 |
LIG_TRFH_1 | 192 | 196 | PF08558 | 0.640 |
MOD_CDC14_SPxK_1 | 137 | 140 | PF00782 | 0.719 |
MOD_CDK_SPxK_1 | 134 | 140 | PF00069 | 0.727 |
MOD_CDK_SPxK_1 | 81 | 87 | PF00069 | 0.677 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.725 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.538 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.619 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.682 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.596 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.653 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.590 |
MOD_N-GLC_1 | 142 | 147 | PF02516 | 0.673 |
MOD_N-GLC_1 | 234 | 239 | PF02516 | 0.664 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.636 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.717 |
MOD_NEK2_2 | 209 | 214 | PF00069 | 0.651 |
MOD_PIKK_1 | 238 | 244 | PF00454 | 0.721 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.729 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.707 |
MOD_PKB_1 | 232 | 240 | PF00069 | 0.701 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.683 |
MOD_Plk_1 | 160 | 166 | PF00069 | 0.479 |
MOD_Plk_1 | 253 | 259 | PF00069 | 0.596 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.688 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.686 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.598 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.682 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.687 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.677 |
TRG_DiLeu_BaEn_1 | 61 | 66 | PF01217 | 0.611 |
TRG_ER_diArg_1 | 180 | 182 | PF00400 | 0.694 |
TRG_ER_diArg_1 | 231 | 234 | PF00400 | 0.694 |
TRG_ER_diArg_1 | 94 | 97 | PF00400 | 0.598 |
TRG_NLS_MonoExtN_4 | 92 | 98 | PF00514 | 0.588 |
TRG_Pf-PMV_PEXEL_1 | 211 | 216 | PF00026 | 0.683 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P385 | Leptomonas seymouri | 58% | 95% |
A0A1X0P111 | Trypanosomatidae | 31% | 75% |
A0A422NCP6 | Trypanosoma rangeli | 30% | 89% |
A4HLJ1 | Leishmania braziliensis | 68% | 94% |
A4HLJ3 | Leishmania braziliensis | 69% | 94% |
A4I8Z9 | Leishmania infantum | 100% | 100% |
E9B3W8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4Q456 | Leishmania major | 94% | 100% |