Nucleic acid binding, Uncharacterized
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: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: A0A3S7X912
Term | Name | Level | Count |
---|---|---|---|
GO:0000447 | endonucleolytic cleavage in ITS1 to separate SSU-rRNA from 5.8S rRNA and LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 1 |
GO:0000469 | cleavage involved in rRNA processing | 7 | 1 |
GO:0000472 | endonucleolytic cleavage to generate mature 5'-end of SSU-rRNA from (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 1 |
GO:0000478 | endonucleolytic cleavage involved in rRNA processing | 8 | 1 |
GO:0000479 | endonucleolytic cleavage of tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 9 | 1 |
GO:0000480 | endonucleolytic cleavage in 5'-ETS of tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 1 |
GO:0000966 | RNA 5'-end processing | 7 | 1 |
GO:0000967 | rRNA 5'-end processing | 9 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 1 |
GO:0034462 | small-subunit processome assembly | 7 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034471 | ncRNA 5'-end processing | 8 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0036260 | RNA capping | 7 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:0090305 | nucleic acid phosphodiester bond hydrolysis | 5 | 1 |
GO:0090501 | RNA phosphodiester bond hydrolysis | 6 | 1 |
GO:0090502 | RNA phosphodiester bond hydrolysis, endonucleolytic | 7 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 8 |
GO:0003723 | RNA binding | 4 | 7 |
GO:0005488 | binding | 1 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 170 | 174 | PF00656 | 0.670 |
CLV_C14_Caspase3-7 | 74 | 78 | PF00656 | 0.462 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 155 | 157 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.741 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.434 |
CLV_PCSK_FUR_1 | 125 | 129 | PF00082 | 0.427 |
CLV_PCSK_FUR_1 | 94 | 98 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.753 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.432 |
CLV_PCSK_PC1ET2_1 | 123 | 125 | PF00082 | 0.526 |
CLV_PCSK_PC1ET2_1 | 159 | 161 | PF00082 | 0.592 |
CLV_PCSK_PC1ET2_1 | 227 | 229 | PF00082 | 0.663 |
CLV_PCSK_PC1ET2_1 | 93 | 95 | PF00082 | 0.439 |
CLV_PCSK_PC7_1 | 156 | 162 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.627 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.447 |
DEG_SPOP_SBC_1 | 204 | 208 | PF00917 | 0.551 |
DOC_MAPK_gen_1 | 24 | 33 | PF00069 | 0.582 |
DOC_MAPK_gen_1 | 42 | 49 | PF00069 | 0.451 |
DOC_MAPK_MEF2A_6 | 27 | 35 | PF00069 | 0.458 |
DOC_MAPK_MEF2A_6 | 54 | 63 | PF00069 | 0.502 |
DOC_PP1_RVXF_1 | 30 | 36 | PF00149 | 0.454 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.702 |
DOC_USP7_UBL2_3 | 205 | 209 | PF12436 | 0.640 |
LIG_AP2alpha_1 | 107 | 111 | PF02296 | 0.411 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.594 |
LIG_BIR_III_4 | 175 | 179 | PF00653 | 0.609 |
LIG_deltaCOP1_diTrp_1 | 67 | 72 | PF00928 | 0.424 |
LIG_LIR_Apic_2 | 5 | 11 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 112 | 120 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 67 | 75 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 112 | 116 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 67 | 72 | PF02991 | 0.424 |
LIG_Pex14_1 | 103 | 107 | PF04695 | 0.344 |
LIG_Pex14_2 | 107 | 111 | PF04695 | 0.434 |
LIG_SH2_CRK | 8 | 12 | PF00017 | 0.481 |
LIG_SH2_GRB2like | 18 | 21 | PF00017 | 0.468 |
LIG_SH2_NCK_1 | 8 | 12 | PF00017 | 0.481 |
LIG_SH2_SRC | 8 | 11 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 18 | 21 | PF00017 | 0.443 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.473 |
LIG_UBA3_1 | 60 | 66 | PF00899 | 0.492 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.700 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.621 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.368 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.517 |
MOD_Cter_Amidation | 121 | 124 | PF01082 | 0.465 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.679 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.768 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.537 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.614 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.635 |
MOD_N-GLC_1 | 181 | 186 | PF02516 | 0.537 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.458 |
MOD_PIKK_1 | 9 | 15 | PF00454 | 0.434 |
MOD_PKB_1 | 193 | 201 | PF00069 | 0.610 |
MOD_Plk_1 | 137 | 143 | PF00069 | 0.517 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.526 |
MOD_Plk_2-3 | 109 | 115 | PF00069 | 0.443 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.428 |
TRG_DiLeu_BaLyEn_6 | 56 | 61 | PF01217 | 0.503 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 99 | 102 | PF00928 | 0.479 |
TRG_ER_diArg_1 | 124 | 127 | PF00400 | 0.424 |
TRG_ER_diArg_1 | 145 | 147 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 160 | 163 | PF00400 | 0.617 |
TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.692 |
TRG_ER_diArg_1 | 41 | 43 | PF00400 | 0.358 |
TRG_ER_diArg_1 | 54 | 56 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 94 | 97 | PF00400 | 0.426 |
TRG_ER_FFAT_2 | 67 | 77 | PF00635 | 0.443 |
TRG_NLS_Bipartite_1 | 146 | 163 | PF00514 | 0.539 |
TRG_NLS_MonoExtC_3 | 122 | 127 | PF00514 | 0.473 |
TRG_NLS_MonoExtC_3 | 155 | 160 | PF00514 | 0.530 |
TRG_NLS_MonoExtC_3 | 223 | 228 | PF00514 | 0.677 |
TRG_NLS_MonoExtC_3 | 50 | 55 | PF00514 | 0.581 |
TRG_NLS_MonoExtC_3 | 92 | 97 | PF00514 | 0.418 |
TRG_NLS_MonoExtN_4 | 156 | 163 | PF00514 | 0.641 |
TRG_NLS_MonoExtN_4 | 222 | 228 | PF00514 | 0.627 |
TRG_NLS_MonoExtN_4 | 48 | 55 | PF00514 | 0.579 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NJ36 | Trypanosomatidae | 52% | 85% |
A0A3R7N8I1 | Trypanosoma rangeli | 56% | 100% |
A3LVD5 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 25% | 67% |
A4HMG2 | Leishmania braziliensis | 84% | 100% |
A4IB33 | Leishmania infantum | 100% | 100% |
E9AEW3 | Leishmania major | 95% | 100% |
E9B619 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
O74362 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 69% |
P53743 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 73% |
Q0UM32 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 29% | 71% |
Q2GZQ4 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 28% | 70% |
Q54BL2 | Dictyostelium discoideum | 25% | 78% |
Q59YL9 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 25% | 72% |
Q6BSS5 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 24% | 77% |
Q6CSP8 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 26% | 79% |
Q75DA3 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 26% | 74% |
Q7S8W7 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 28% | 68% |