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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q4K8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 168 | 172 | PF00656 | 0.675 |
CLV_C14_Caspase3-7 | 68 | 72 | PF00656 | 0.699 |
CLV_NRD_NRD_1 | 140 | 142 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.317 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.700 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.701 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.566 |
CLV_PCSK_PC1ET2_1 | 121 | 123 | PF00082 | 0.708 |
CLV_PCSK_PC1ET2_1 | 45 | 47 | PF00082 | 0.566 |
CLV_PCSK_PC7_1 | 117 | 123 | PF00082 | 0.717 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.612 |
DOC_PP4_FxxP_1 | 135 | 138 | PF00568 | 0.719 |
DOC_PP4_FxxP_1 | 51 | 54 | PF00568 | 0.700 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.586 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.783 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.699 |
LIG_14-3-3_CanoR_1 | 115 | 121 | PF00244 | 0.709 |
LIG_14-3-3_CanoR_1 | 140 | 146 | PF00244 | 0.701 |
LIG_14-3-3_CanoR_1 | 251 | 260 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 269 | 275 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 57 | 65 | PF00244 | 0.689 |
LIG_BIR_III_4 | 169 | 173 | PF00653 | 0.666 |
LIG_Clathr_ClatBox_1 | 184 | 188 | PF01394 | 0.660 |
LIG_Clathr_ClatBox_1 | 85 | 89 | PF01394 | 0.744 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.663 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.754 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.644 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.562 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.545 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.684 |
LIG_FHA_2 | 91 | 97 | PF00498 | 0.634 |
LIG_LIR_Apic_2 | 195 | 201 | PF02991 | 0.627 |
LIG_LIR_Apic_2 | 48 | 54 | PF02991 | 0.691 |
LIG_LIR_Gen_1 | 180 | 189 | PF02991 | 0.744 |
LIG_LIR_Nem_3 | 100 | 105 | PF02991 | 0.656 |
LIG_LIR_Nem_3 | 161 | 166 | PF02991 | 0.638 |
LIG_LIR_Nem_3 | 180 | 184 | PF02991 | 0.683 |
LIG_LIR_Nem_3 | 256 | 261 | PF02991 | 0.667 |
LIG_MYND_1 | 50 | 54 | PF01753 | 0.576 |
LIG_Rb_LxCxE_1 | 180 | 202 | PF01857 | 0.670 |
LIG_SH2_STAP1 | 181 | 185 | PF00017 | 0.609 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.627 |
LIG_SH3_3 | 34 | 40 | PF00018 | 0.612 |
LIG_TRAF2_1 | 236 | 239 | PF00917 | 0.654 |
LIG_TRAF2_1 | 92 | 95 | PF00917 | 0.588 |
LIG_TRFH_1 | 134 | 138 | PF08558 | 0.724 |
LIG_UBA3_1 | 85 | 91 | PF00899 | 0.555 |
MOD_CDC14_SPxK_1 | 159 | 162 | PF00782 | 0.786 |
MOD_CDK_SPxK_1 | 156 | 162 | PF00069 | 0.785 |
MOD_CDK_SPxxK_3 | 50 | 57 | PF00069 | 0.697 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.747 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.749 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.473 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.737 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.541 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.542 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.677 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.527 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.698 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.692 |
MOD_GlcNHglycan | 214 | 219 | PF01048 | 0.327 |
MOD_GlcNHglycan | 226 | 231 | PF01048 | 0.566 |
MOD_GlcNHglycan | 237 | 243 | PF01048 | 0.658 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.763 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.674 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.699 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.560 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.713 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.717 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.634 |
MOD_NEK2_2 | 10 | 15 | PF00069 | 0.655 |
MOD_PK_1 | 141 | 147 | PF00069 | 0.650 |
MOD_PKA_1 | 139 | 145 | PF00069 | 0.699 |
MOD_PKA_1 | 45 | 51 | PF00069 | 0.563 |
MOD_PKA_2 | 116 | 122 | PF00069 | 0.739 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.700 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.754 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.640 |
MOD_PKB_1 | 139 | 147 | PF00069 | 0.677 |
MOD_Plk_1 | 267 | 273 | PF00069 | 0.641 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.782 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.685 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.560 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.785 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.699 |
MOD_SUMO_rev_2 | 84 | 93 | PF00179 | 0.541 |
TRG_DiLeu_BaEn_1 | 180 | 185 | PF01217 | 0.672 |
TRG_DiLeu_BaEn_4 | 126 | 132 | PF01217 | 0.751 |
TRG_DiLeu_BaLyEn_6 | 173 | 178 | PF01217 | 0.662 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.632 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.669 |
TRG_ER_diArg_1 | 122 | 125 | PF00400 | 0.670 |
TRG_ER_diArg_1 | 138 | 141 | PF00400 | 0.605 |
TRG_ER_diArg_1 | 20 | 22 | PF00400 | 0.622 |
TRG_NES_CRM1_1 | 96 | 111 | PF08389 | 0.616 |
TRG_NLS_MonoExtC_3 | 120 | 126 | PF00514 | 0.674 |
TRG_Pf-PMV_PEXEL_1 | 176 | 180 | PF00026 | 0.726 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5U4 | Leptomonas seymouri | 44% | 82% |
A0A3S7X690 | Leishmania donovani | 88% | 100% |
A4HL52 | Leishmania braziliensis | 68% | 100% |
A4I8N1 | Leishmania infantum | 88% | 100% |
D0A4K8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 74% |
E9B3J3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |