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: 10 |
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: 3 |
NetGPI | no | yes: 0, no: 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030684 | preribosome | 3 | 1 |
GO:0030687 | preribosome, large subunit precursor | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3S5H611
Term | Name | Level | Count |
---|---|---|---|
GO:0000027 | ribosomal large subunit assembly | 7 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0019843 | rRNA binding | 5 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.699 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.670 |
CLV_PCSK_PC1ET2_1 | 331 | 333 | PF00082 | 0.670 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.375 |
DEG_Kelch_Keap1_1 | 173 | 178 | PF01344 | 0.538 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.670 |
DOC_CYCLIN_yCln2_LP_2 | 30 | 36 | PF00134 | 0.375 |
DOC_PP2B_LxvP_1 | 30 | 33 | PF13499 | 0.375 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.708 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.649 |
LIG_14-3-3_CanoR_1 | 26 | 33 | PF00244 | 0.375 |
LIG_Actin_WH2_2 | 12 | 28 | PF00022 | 0.375 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.389 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.476 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.542 |
LIG_Integrin_RGD_1 | 243 | 245 | PF01839 | 0.693 |
LIG_LIR_Apic_2 | 90 | 95 | PF02991 | 0.375 |
LIG_LIR_LC3C_4 | 41 | 44 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.375 |
LIG_SH2_PTP2 | 92 | 95 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.660 |
LIG_TRAF2_1 | 110 | 113 | PF00917 | 0.733 |
LIG_TRAF2_1 | 146 | 149 | PF00917 | 0.700 |
LIG_TRAF2_1 | 176 | 179 | PF00917 | 0.546 |
LIG_WRC_WIRS_1 | 43 | 48 | PF05994 | 0.375 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.682 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.553 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.707 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.541 |
MOD_Cter_Amidation | 329 | 332 | PF01082 | 0.672 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.688 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.647 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.462 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.701 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.491 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.520 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.520 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.375 |
MOD_Plk_1 | 75 | 81 | PF00069 | 0.375 |
MOD_Plk_2-3 | 113 | 119 | PF00069 | 0.701 |
MOD_Plk_2-3 | 122 | 128 | PF00069 | 0.605 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.455 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.650 |
MOD_SUMO_rev_2 | 41 | 51 | PF00179 | 0.375 |
TRG_ER_diArg_1 | 332 | 335 | PF00400 | 0.672 |
TRG_NLS_MonoExtN_4 | 328 | 335 | PF00514 | 0.673 |