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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043228 | non-membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: E9AN96
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 1 |
GO:0022613 | ribonucleoprotein complex biogenesis | 4 | 1 |
GO:0042273 | ribosomal large subunit biogenesis | 5 | 1 |
GO:0044085 | cellular component biogenesis | 3 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.438 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.426 |
CLV_PCSK_PC1ET2_1 | 134 | 136 | PF00082 | 0.404 |
CLV_PCSK_PC1ET2_1 | 28 | 30 | PF00082 | 0.455 |
CLV_PCSK_PC1ET2_1 | 79 | 81 | PF00082 | 0.578 |
CLV_PCSK_PC7_1 | 85 | 91 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.537 |
DOC_MAPK_gen_1 | 9 | 18 | PF00069 | 0.532 |
DOC_MAPK_RevD_3 | 66 | 80 | PF00069 | 0.559 |
DOC_PP4_FxxP_1 | 185 | 188 | PF00568 | 0.523 |
DOC_USP7_UBL2_3 | 24 | 28 | PF12436 | 0.363 |
DOC_USP7_UBL2_3 | 5 | 9 | PF12436 | 0.559 |
DOC_USP7_UBL2_3 | 79 | 83 | PF12436 | 0.585 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.546 |
LIG_14-3-3_CanoR_1 | 135 | 139 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 45 | 51 | PF00244 | 0.511 |
LIG_deltaCOP1_diTrp_1 | 175 | 185 | PF00928 | 0.409 |
LIG_EH_1 | 142 | 146 | PF12763 | 0.314 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.524 |
LIG_LIR_Apic_2 | 183 | 188 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 58 | 68 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 176 | 182 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.466 |
LIG_PCNA_PIPBox_1 | 153 | 162 | PF02747 | 0.349 |
LIG_PCNA_yPIPBox_3 | 150 | 160 | PF02747 | 0.271 |
LIG_Pex14_2 | 167 | 171 | PF04695 | 0.436 |
LIG_PTAP_UEV_1 | 69 | 74 | PF05743 | 0.421 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.429 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.405 |
LIG_TRAF2_1 | 115 | 118 | PF00917 | 0.341 |
LIG_TRAF2_1 | 99 | 102 | PF00917 | 0.381 |
MOD_CDK_SPK_2 | 4 | 9 | PF00069 | 0.546 |
MOD_CDK_SPxxK_3 | 4 | 11 | PF00069 | 0.545 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.309 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.554 |
MOD_Cter_Amidation | 21 | 24 | PF01082 | 0.453 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.605 |
MOD_GlcNHglycan | 69 | 73 | PF01048 | 0.481 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.494 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.577 |
MOD_N-GLC_1 | 53 | 58 | PF02516 | 0.555 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.445 |
MOD_PKA_1 | 134 | 140 | PF00069 | 0.404 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.404 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.516 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.413 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.545 |
MOD_SUMO_for_1 | 160 | 163 | PF00179 | 0.490 |
MOD_SUMO_rev_2 | 127 | 136 | PF00179 | 0.326 |
TRG_DiLeu_BaEn_4 | 93 | 99 | PF01217 | 0.463 |
TRG_ER_diArg_1 | 29 | 31 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 89 | 91 | PF00400 | 0.448 |
TRG_NLS_Bipartite_1 | 13 | 32 | PF00514 | 0.475 |
TRG_NLS_MonoExtN_4 | 79 | 84 | PF00514 | 0.575 |
TRG_Pf-PMV_PEXEL_1 | 150 | 155 | PF00026 | 0.271 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HY36 | Leptomonas seymouri | 91% | 100% |
A0A1X0NQN2 | Trypanosomatidae | 69% | 100% |
A0A3R7LG34 | Trypanosoma rangeli | 67% | 100% |
A0A3S7WR83 | Leishmania donovani | 98% | 100% |
A4H674 | Leishmania braziliensis | 94% | 100% |
A4HUJ8 | Leishmania infantum | 98% | 100% |
C9ZVM3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
Q4QHC8 | Leishmania major | 96% | 100% |
V5BJL8 | Trypanosoma cruzi | 66% | 100% |