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: A0A3Q8IFW9
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 | 0.513 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.209 |
CLV_NRD_NRD_1 | 280 | 282 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 91 | 93 | PF00675 | 0.489 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 279 | 281 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.440 |
CLV_PCSK_PC1ET2_1 | 279 | 281 | PF00082 | 0.570 |
CLV_PCSK_PC1ET2_1 | 285 | 287 | PF00082 | 0.523 |
CLV_PCSK_PC1ET2_1 | 304 | 306 | PF00082 | 0.329 |
CLV_PCSK_PC1ET2_1 | 339 | 341 | PF00082 | 0.552 |
CLV_PCSK_PC1ET2_1 | 95 | 97 | PF00082 | 0.440 |
CLV_PCSK_PC7_1 | 281 | 287 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.219 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.576 |
CLV_Separin_Metazoa | 15 | 19 | PF03568 | 0.503 |
DOC_ANK_TNKS_1 | 30 | 37 | PF00023 | 0.406 |
DOC_MAPK_gen_1 | 201 | 209 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 345 | 354 | PF00069 | 0.483 |
DOC_MAPK_NFAT4_5 | 345 | 353 | PF00069 | 0.482 |
DOC_PP4_FxxP_1 | 181 | 184 | PF00568 | 0.443 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.475 |
DOC_USP7_UBL2_3 | 139 | 143 | PF12436 | 0.575 |
DOC_USP7_UBL2_3 | 275 | 279 | PF12436 | 0.547 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.581 |
LIG_14-3-3_CanoR_1 | 214 | 219 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 38 | 47 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 85 | 91 | PF00244 | 0.437 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.421 |
LIG_BIR_III_2 | 135 | 139 | PF00653 | 0.563 |
LIG_DLG_GKlike_1 | 214 | 221 | PF00625 | 0.499 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.409 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.452 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.597 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.446 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.409 |
LIG_FHA_2 | 229 | 235 | PF00498 | 0.416 |
LIG_GBD_Chelix_1 | 199 | 207 | PF00786 | 0.299 |
LIG_Integrin_RGD_1 | 133 | 135 | PF01839 | 0.612 |
LIG_Integrin_RGD_1 | 265 | 267 | PF01839 | 0.629 |
LIG_LIR_Apic_2 | 180 | 184 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 215 | 224 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 239 | 250 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 73 | 80 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 215 | 221 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 239 | 245 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 73 | 77 | PF02991 | 0.419 |
LIG_PCNA_PIPBox_1 | 192 | 201 | PF02747 | 0.424 |
LIG_PCNA_yPIPBox_3 | 192 | 202 | PF02747 | 0.424 |
LIG_SH2_CRK | 246 | 250 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 246 | 250 | PF00017 | 0.434 |
LIG_SH2_STAP1 | 65 | 69 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.409 |
LIG_SH3_CIN85_PxpxPR_1 | 291 | 296 | PF14604 | 0.637 |
LIG_TRAF2_1 | 319 | 322 | PF00917 | 0.508 |
LIG_UBA3_1 | 195 | 202 | PF00899 | 0.419 |
LIG_WRC_WIRS_1 | 178 | 183 | PF05994 | 0.424 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.530 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.451 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.478 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.419 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.499 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.495 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.476 |
MOD_Cter_Amidation | 277 | 280 | PF01082 | 0.551 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.530 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.546 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.279 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.536 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.491 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.485 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.459 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.620 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.492 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.435 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.557 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.492 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.454 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.433 |
MOD_NEK2_2 | 70 | 75 | PF00069 | 0.428 |
MOD_PIKK_1 | 38 | 44 | PF00454 | 0.482 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.495 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.609 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.521 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.441 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.435 |
MOD_PKB_1 | 214 | 222 | PF00069 | 0.499 |
MOD_Plk_1 | 350 | 356 | PF00069 | 0.550 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.582 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.512 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.570 |
MOD_SUMO_for_1 | 284 | 287 | PF00179 | 0.630 |
MOD_SUMO_rev_2 | 129 | 138 | PF00179 | 0.547 |
TRG_DiLeu_BaEn_1 | 322 | 327 | PF01217 | 0.470 |
TRG_DiLeu_BaLyEn_6 | 232 | 237 | PF01217 | 0.512 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.421 |
TRG_ER_diArg_1 | 280 | 282 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 291 | 294 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 30 | 33 | PF00400 | 0.392 |
TRG_Pf-PMV_PEXEL_1 | 316 | 321 | PF00026 | 0.521 |
TRG_Pf-PMV_PEXEL_1 | 38 | 42 | PF00026 | 0.449 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3A3 | Leptomonas seymouri | 76% | 99% |
A0A0S4ILF0 | Bodo saltans | 47% | 100% |
A0A1X0P2R4 | Trypanosomatidae | 53% | 100% |
A0A422NW52 | Trypanosoma rangeli | 52% | 100% |
A4HIF7 | Leishmania braziliensis | 82% | 100% |
A4I5Q3 | Leishmania infantum | 100% | 100% |
C9ZR22 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9B0Z8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
G0S920 | Chaetomium thermophilum (strain DSM 1495 / CBS 144.50 / IMI 039719) | 25% | 69% |
O59811 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 80% |
P38344 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 94% |
Q06709 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 86% |
Q4Q768 | Leishmania major | 94% | 100% |
Q8H1G5 | Arabidopsis thaliana | 23% | 92% |
Q9ZQ18 | Arabidopsis thaliana | 24% | 94% |
V5BC84 | Trypanosoma cruzi | 53% | 100% |