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:0005737 | cytoplasm | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
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: A4HIF7
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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0005488 | binding | 1 | 12 |
GO:0008270 | zinc ion binding | 6 | 10 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0046914 | transition metal ion binding | 5 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 91 | 93 | PF00675 | 0.521 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 279 | 281 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.586 |
CLV_PCSK_PC1ET2_1 | 279 | 281 | PF00082 | 0.606 |
CLV_PCSK_PC1ET2_1 | 284 | 286 | PF00082 | 0.607 |
CLV_PCSK_PC1ET2_1 | 303 | 305 | PF00082 | 0.344 |
CLV_PCSK_PC1ET2_1 | 338 | 340 | PF00082 | 0.590 |
CLV_PCSK_PC7_1 | 280 | 286 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 320 | 324 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.371 |
DOC_ANK_TNKS_1 | 30 | 37 | PF00023 | 0.468 |
DOC_MAPK_gen_1 | 137 | 145 | PF00069 | 0.484 |
DOC_MAPK_gen_1 | 200 | 208 | PF00069 | 0.451 |
DOC_MAPK_MEF2A_6 | 137 | 145 | PF00069 | 0.543 |
DOC_MAPK_MEF2A_6 | 344 | 353 | PF00069 | 0.543 |
DOC_MAPK_NFAT4_5 | 344 | 352 | PF00069 | 0.626 |
DOC_PP4_FxxP_1 | 180 | 183 | PF00568 | 0.453 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.585 |
DOC_USP7_UBL2_3 | 138 | 142 | PF12436 | 0.624 |
DOC_USP7_UBL2_3 | 274 | 278 | PF12436 | 0.688 |
DOC_USP7_UBL2_3 | 357 | 361 | PF12436 | 0.510 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.603 |
LIG_14-3-3_CanoR_1 | 215 | 221 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 38 | 47 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 75 | 81 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 85 | 91 | PF00244 | 0.457 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.353 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.456 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.459 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.383 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.588 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.641 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.514 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.447 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.567 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.434 |
LIG_FHA_2 | 53 | 59 | PF00498 | 0.473 |
LIG_Integrin_RGD_1 | 133 | 135 | PF01839 | 0.750 |
LIG_Integrin_RGD_1 | 264 | 266 | PF01839 | 0.661 |
LIG_LIR_Gen_1 | 238 | 249 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 214 | 220 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 238 | 244 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 73 | 77 | PF02991 | 0.454 |
LIG_PTB_Apo_2 | 68 | 75 | PF02174 | 0.378 |
LIG_SH2_STAP1 | 21 | 25 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 245 | 249 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 65 | 69 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.453 |
LIG_TRAF2_1 | 12 | 15 | PF00917 | 0.378 |
LIG_TRAF2_1 | 41 | 44 | PF00917 | 0.412 |
LIG_UBA3_1 | 194 | 201 | PF00899 | 0.449 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.549 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.479 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.464 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.435 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.547 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.355 |
MOD_CK2_1 | 38 | 44 | PF00069 | 0.458 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.529 |
MOD_Cter_Amidation | 276 | 279 | PF01082 | 0.687 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.545 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.586 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.573 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.540 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.544 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.597 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.322 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.482 |
MOD_N-GLC_1 | 178 | 183 | PF02516 | 0.178 |
MOD_N-GLC_1 | 59 | 64 | PF02516 | 0.558 |
MOD_N-GLC_1 | 70 | 75 | PF02516 | 0.147 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.567 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.378 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.523 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.498 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.322 |
MOD_NEK2_2 | 70 | 75 | PF00069 | 0.464 |
MOD_OFUCOSY | 61 | 67 | PF10250 | 0.332 |
MOD_PIKK_1 | 325 | 331 | PF00454 | 0.540 |
MOD_PIKK_1 | 38 | 44 | PF00454 | 0.539 |
MOD_PK_1 | 303 | 309 | PF00069 | 0.359 |
MOD_PKA_1 | 303 | 309 | PF00069 | 0.482 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.388 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.528 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.638 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.585 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.559 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.458 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.379 |
MOD_Plk_1 | 178 | 184 | PF00069 | 0.387 |
MOD_Plk_1 | 70 | 76 | PF00069 | 0.378 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.589 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.359 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.426 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.539 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.594 |
MOD_SUMO_for_1 | 12 | 15 | PF00179 | 0.378 |
MOD_SUMO_for_1 | 283 | 286 | PF00179 | 0.686 |
MOD_SUMO_rev_2 | 129 | 139 | PF00179 | 0.644 |
TRG_DiLeu_BaEn_1 | 321 | 326 | PF01217 | 0.525 |
TRG_DiLeu_BaLyEn_6 | 231 | 236 | PF01217 | 0.539 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.453 |
TRG_ER_diArg_1 | 290 | 293 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 30 | 33 | PF00400 | 0.452 |
TRG_Pf-PMV_PEXEL_1 | 320 | 324 | PF00026 | 0.555 |
TRG_Pf-PMV_PEXEL_1 | 38 | 42 | PF00026 | 0.508 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3A3 | Leptomonas seymouri | 74% | 99% |
A0A0S4ILF0 | Bodo saltans | 46% | 100% |
A0A1X0P2R4 | Trypanosomatidae | 54% | 100% |
A0A3Q8IFW9 | Leishmania donovani | 82% | 100% |
A0A422NW52 | Trypanosoma rangeli | 53% | 100% |
A4I5Q3 | Leishmania infantum | 82% | 100% |
C9ZR22 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
E9B0Z8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
G0S920 | Chaetomium thermophilum (strain DSM 1495 / CBS 144.50 / IMI 039719) | 24% | 69% |
O59811 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 80% |
Q06709 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 86% |
Q4Q768 | Leishmania major | 82% | 100% |
Q8H1G5 | Arabidopsis thaliana | 25% | 92% |
Q9ZQ18 | Arabidopsis thaliana | 25% | 94% |
V5BC84 | Trypanosoma cruzi | 55% | 100% |