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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AMW6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 181 | 187 | PF00089 | 0.679 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 279 | 281 | PF00675 | 0.462 |
CLV_PCSK_FUR_1 | 228 | 232 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.556 |
CLV_PCSK_PC1ET2_1 | 100 | 102 | PF00082 | 0.523 |
CLV_PCSK_PC1ET2_1 | 166 | 168 | PF00082 | 0.480 |
CLV_PCSK_PC1ET2_1 | 281 | 283 | PF00082 | 0.707 |
CLV_PCSK_PC1ET2_1 | 48 | 50 | PF00082 | 0.574 |
CLV_PCSK_PC7_1 | 173 | 179 | PF00082 | 0.511 |
CLV_PCSK_PC7_1 | 277 | 283 | PF00082 | 0.804 |
CLV_PCSK_PC7_1 | 96 | 102 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.524 |
CLV_Separin_Metazoa | 252 | 256 | PF03568 | 0.582 |
DEG_SCF_SKP2-CKS1_1 | 185 | 192 | PF00560 | 0.560 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.664 |
DOC_USP7_UBL2_3 | 14 | 18 | PF12436 | 0.677 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.556 |
LIG_14-3-3_CanoR_1 | 145 | 152 | PF00244 | 0.587 |
LIG_deltaCOP1_diTrp_1 | 88 | 94 | PF00928 | 0.449 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.511 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.510 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.523 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.531 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.527 |
LIG_LIR_Nem_3 | 88 | 94 | PF02991 | 0.479 |
LIG_PDZ_Class_3 | 282 | 287 | PF00595 | 0.694 |
LIG_SH2_STAP1 | 123 | 127 | PF00017 | 0.633 |
LIG_SH2_STAP1 | 256 | 260 | PF00017 | 0.522 |
LIG_SH2_STAP1 | 70 | 74 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 70 | 73 | PF00017 | 0.642 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.681 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.500 |
LIG_TRAF2_1 | 249 | 252 | PF00917 | 0.563 |
MOD_CDK_SPxK_1 | 186 | 192 | PF00069 | 0.561 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.567 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.520 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.526 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.531 |
MOD_Cter_Amidation | 278 | 281 | PF01082 | 0.750 |
MOD_Cter_Amidation | 98 | 101 | PF01082 | 0.509 |
MOD_GlcNHglycan | 156 | 160 | PF01048 | 0.534 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.549 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.518 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.664 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.527 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.664 |
MOD_N-GLC_1 | 116 | 121 | PF02516 | 0.546 |
MOD_N-GLC_1 | 207 | 212 | PF02516 | 0.504 |
MOD_N-GLC_1 | 240 | 245 | PF02516 | 0.550 |
MOD_N-GLC_1 | 79 | 84 | PF02516 | 0.501 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.561 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.504 |
MOD_PIKK_1 | 128 | 134 | PF00454 | 0.539 |
MOD_PIKK_1 | 233 | 239 | PF00454 | 0.602 |
MOD_PKA_1 | 100 | 106 | PF00069 | 0.498 |
MOD_PKA_1 | 231 | 237 | PF00069 | 0.569 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.546 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.521 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.592 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.534 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.645 |
MOD_Plk_1 | 207 | 213 | PF00069 | 0.500 |
MOD_Plk_1 | 79 | 85 | PF00069 | 0.505 |
MOD_Plk_2-3 | 79 | 85 | PF00069 | 0.496 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.663 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.390 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.561 |
TRG_ER_diArg_1 | 105 | 108 | PF00400 | 0.690 |
TRG_ER_diArg_1 | 176 | 178 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 182 | 184 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 227 | 230 | PF00400 | 0.612 |
TRG_ER_diArg_1 | 264 | 266 | PF00400 | 0.562 |
TRG_ER_KDEL_1 | 284 | 287 | PF00810 | 0.693 |
TRG_NLS_MonoCore_2 | 45 | 50 | PF00514 | 0.683 |
TRG_NLS_MonoExtC_3 | 45 | 51 | PF00514 | 0.682 |
TRG_NLS_MonoExtN_4 | 264 | 270 | PF00514 | 0.618 |
TRG_Pf-PMV_PEXEL_1 | 10 | 15 | PF00026 | 0.637 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2W8 | Leptomonas seymouri | 85% | 98% |
A0A0S4JUY7 | Bodo saltans | 54% | 100% |
A0A1X0NHZ1 | Trypanosomatidae | 57% | 93% |
A0A3S7WQW2 | Leishmania donovani | 97% | 100% |
A0A422NZP9 | Trypanosoma rangeli | 63% | 100% |
A4H5U3 | Leishmania braziliensis | 92% | 100% |
A4HU37 | Leishmania infantum | 97% | 100% |
D0A9L6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 95% |
Q4QHR0 | Leishmania major | 94% | 100% |
V5BMM5 | Trypanosoma cruzi | 63% | 99% |