Nucleic acid binding, PUF1 PUF1
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: 1, no: 18 |
NetGPI | no | yes: 0, no: 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4ICY3
Term | Name | Level | Count |
---|---|---|---|
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 20 |
GO:0003723 | RNA binding | 4 | 20 |
GO:0005488 | binding | 1 | 20 |
GO:0097159 | organic cyclic compound binding | 2 | 20 |
GO:1901363 | heterocyclic compound binding | 2 | 20 |
GO:0003729 | mRNA binding | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 442 | 444 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 449 | 451 | PF00675 | 0.468 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 449 | 451 | PF00082 | 0.493 |
CLV_PCSK_PC1ET2_1 | 44 | 46 | PF00082 | 0.693 |
CLV_PCSK_PC7_1 | 445 | 451 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.490 |
DEG_APCC_DBOX_1 | 342 | 350 | PF00400 | 0.375 |
DEG_APCC_DBOX_1 | 74 | 82 | PF00400 | 0.498 |
DEG_COP1_1 | 324 | 334 | PF00400 | 0.440 |
DOC_CYCLIN_RxL_1 | 443 | 456 | PF00134 | 0.423 |
DOC_CYCLIN_yCln2_LP_2 | 472 | 475 | PF00134 | 0.576 |
DOC_PP2B_LxvP_1 | 381 | 384 | PF13499 | 0.381 |
DOC_PP2B_LxvP_1 | 472 | 475 | PF13499 | 0.726 |
DOC_PP4_FxxP_1 | 148 | 151 | PF00568 | 0.373 |
DOC_PP4_FxxP_1 | 510 | 513 | PF00568 | 0.682 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.389 |
DOC_USP7_MATH_1 | 422 | 426 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 490 | 494 | PF00917 | 0.678 |
DOC_USP7_UBL2_3 | 435 | 439 | PF12436 | 0.391 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.357 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.389 |
LIG_14-3-3_CanoR_1 | 183 | 191 | PF00244 | 0.373 |
LIG_Actin_WH2_2 | 284 | 299 | PF00022 | 0.356 |
LIG_Actin_WH2_2 | 354 | 369 | PF00022 | 0.267 |
LIG_Actin_WH2_2 | 413 | 430 | PF00022 | 0.416 |
LIG_Actin_WH2_2 | 61 | 77 | PF00022 | 0.398 |
LIG_AP2alpha_2 | 301 | 303 | PF02296 | 0.264 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.543 |
LIG_BIR_III_2 | 329 | 333 | PF00653 | 0.438 |
LIG_BIR_III_4 | 121 | 125 | PF00653 | 0.466 |
LIG_BIR_III_4 | 70 | 74 | PF00653 | 0.438 |
LIG_BRCT_BRCA1_1 | 227 | 231 | PF00533 | 0.467 |
LIG_BRCT_BRCA1_1 | 26 | 30 | PF00533 | 0.387 |
LIG_CaM_IQ_9 | 84 | 100 | PF13499 | 0.405 |
LIG_EVH1_2 | 535 | 539 | PF00568 | 0.558 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.494 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.453 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.372 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.365 |
LIG_FHA_2 | 141 | 147 | PF00498 | 0.549 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.494 |
LIG_FHA_2 | 192 | 198 | PF00498 | 0.361 |
LIG_FHA_2 | 404 | 410 | PF00498 | 0.346 |
LIG_FHA_2 | 44 | 50 | PF00498 | 0.613 |
LIG_LIR_Apic_2 | 146 | 151 | PF02991 | 0.375 |
LIG_LIR_Apic_2 | 509 | 513 | PF02991 | 0.714 |
LIG_LIR_Gen_1 | 199 | 209 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 228 | 238 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 249 | 260 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 499 | 508 | PF02991 | 0.669 |
LIG_LIR_Nem_3 | 196 | 201 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 228 | 234 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 249 | 255 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 301 | 306 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 392 | 398 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 499 | 503 | PF02991 | 0.637 |
LIG_MYND_1 | 471 | 475 | PF01753 | 0.736 |
LIG_PCNA_yPIPBox_3 | 214 | 226 | PF02747 | 0.333 |
LIG_PCNA_yPIPBox_3 | 504 | 515 | PF02747 | 0.541 |
LIG_Pex14_2 | 103 | 107 | PF04695 | 0.382 |
LIG_PTAP_UEV_1 | 331 | 336 | PF05743 | 0.430 |
LIG_PTB_Apo_2 | 426 | 433 | PF02174 | 0.355 |
LIG_PTB_Phospho_1 | 426 | 432 | PF10480 | 0.360 |
LIG_SH2_CRK | 201 | 205 | PF00017 | 0.482 |
LIG_SH2_CRK | 476 | 480 | PF00017 | 0.590 |
LIG_SH2_GRB2like | 337 | 340 | PF00017 | 0.379 |
LIG_SH2_NCK_1 | 248 | 252 | PF00017 | 0.384 |
LIG_SH2_STAP1 | 201 | 205 | PF00017 | 0.472 |
LIG_SH2_STAP1 | 248 | 252 | PF00017 | 0.424 |
LIG_SH2_STAP1 | 337 | 341 | PF00017 | 0.408 |
LIG_SH2_STAT3 | 306 | 309 | PF00017 | 0.274 |
LIG_SH2_STAT3 | 337 | 340 | PF00017 | 0.466 |
LIG_SH2_STAT3 | 398 | 401 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 398 | 401 | PF00017 | 0.258 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.494 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.473 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.291 |
LIG_SH3_3 | 329 | 335 | PF00018 | 0.456 |
LIG_SH3_3 | 468 | 474 | PF00018 | 0.666 |
LIG_SH3_3 | 529 | 535 | PF00018 | 0.694 |
LIG_SUMO_SIM_anti_2 | 159 | 167 | PF11976 | 0.364 |
LIG_SUMO_SIM_par_1 | 159 | 167 | PF11976 | 0.384 |
LIG_TRAF2_1 | 194 | 197 | PF00917 | 0.260 |
LIG_TRAF2_1 | 2 | 5 | PF00917 | 0.461 |
LIG_TRAF2_1 | 467 | 470 | PF00917 | 0.723 |
LIG_UBA3_1 | 420 | 428 | PF00899 | 0.425 |
LIG_WRC_WIRS_1 | 507 | 512 | PF05994 | 0.581 |
MOD_CDK_SPxxK_3 | 367 | 374 | PF00069 | 0.399 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.582 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.345 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.538 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.534 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.275 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.310 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.514 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.595 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.511 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.508 |
MOD_GlcNHglycan | 238 | 242 | PF01048 | 0.514 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.759 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.555 |
MOD_GlcNHglycan | 546 | 549 | PF01048 | 0.691 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.485 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.425 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.456 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.426 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.377 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.496 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.279 |
MOD_N-GLC_1 | 122 | 127 | PF02516 | 0.394 |
MOD_N-GLC_1 | 218 | 223 | PF02516 | 0.373 |
MOD_N-GLC_1 | 292 | 297 | PF02516 | 0.371 |
MOD_N-GLC_1 | 318 | 323 | PF02516 | 0.553 |
MOD_N-GLC_1 | 335 | 340 | PF02516 | 0.347 |
MOD_N-GLC_1 | 49 | 54 | PF02516 | 0.592 |
MOD_N-GLC_1 | 544 | 549 | PF02516 | 0.706 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.461 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.435 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.374 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.431 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.315 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.399 |
MOD_PIKK_1 | 411 | 417 | PF00454 | 0.335 |
MOD_PIKK_1 | 459 | 465 | PF00454 | 0.671 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.397 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.460 |
MOD_Plk_1 | 24 | 30 | PF00069 | 0.425 |
MOD_Plk_1 | 292 | 298 | PF00069 | 0.489 |
MOD_Plk_1 | 490 | 496 | PF00069 | 0.739 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.415 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.311 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.405 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.611 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.357 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.383 |
MOD_SUMO_for_1 | 434 | 437 | PF00179 | 0.448 |
MOD_SUMO_rev_2 | 2 | 8 | PF00179 | 0.438 |
MOD_SUMO_rev_2 | 48 | 52 | PF00179 | 0.663 |
TRG_DiLeu_BaEn_1 | 160 | 165 | PF01217 | 0.337 |
TRG_DiLeu_BaLyEn_6 | 130 | 135 | PF01217 | 0.440 |
TRG_DiLeu_BaLyEn_6 | 447 | 452 | PF01217 | 0.425 |
TRG_DiLeu_BaLyEn_6 | 468 | 473 | PF01217 | 0.575 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.321 |
TRG_ER_diArg_1 | 442 | 445 | PF00400 | 0.472 |
TRG_ER_diArg_1 | 449 | 451 | PF00400 | 0.516 |
TRG_Pf-PMV_PEXEL_1 | 166 | 171 | PF00026 | 0.464 |
TRG_Pf-PMV_PEXEL_1 | 19 | 23 | PF00026 | 0.416 |
TRG_Pf-PMV_PEXEL_1 | 374 | 379 | PF00026 | 0.311 |
TRG_Pf-PMV_PEXEL_1 | 45 | 49 | PF00026 | 0.670 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P473 | Leptomonas seymouri | 80% | 99% |
A0A0S4IY52 | Bodo saltans | 29% | 78% |
A0A0S4JMB8 | Bodo saltans | 46% | 79% |
A0A1X0NHM5 | Trypanosomatidae | 29% | 98% |
A0A1X0P8D8 | Trypanosomatidae | 45% | 96% |
A0A3Q8IK20 | Leishmania donovani | 100% | 100% |
A0A3R7NHA6 | Trypanosoma rangeli | 45% | 97% |
A0A422N8V0 | Trypanosoma rangeli | 28% | 100% |
A4HNL0 | Leishmania braziliensis | 90% | 100% |
C9ZII7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 82% |
D0A0Z9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 95% |
D0A2G7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 97% |
E9ASC2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
E9AUS6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
Q4Q274 | Leishmania major | 99% | 100% |
Q4QCQ8 | Leishmania major | 24% | 100% |
V5B1W9 | Trypanosoma cruzi | 29% | 99% |
V5BV90 | Trypanosoma cruzi | 46% | 91% |