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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: E9AKA0
Term | Name | Level | Count |
---|---|---|---|
GO:0001680 | tRNA 3'-terminal CCA addition | 9 | 11 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006399 | tRNA metabolic process | 7 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008033 | tRNA processing | 8 | 11 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0031123 | RNA 3'-end processing | 7 | 12 |
GO:0034470 | ncRNA processing | 7 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034660 | ncRNA metabolic process | 6 | 11 |
GO:0042780 | tRNA 3'-end processing | 8 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071076 | RNA 3' uridylation | 8 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0005488 | binding | 1 | 12 |
GO:0016740 | transferase activity | 2 | 13 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016779 | nucleotidyltransferase activity | 4 | 12 |
GO:0050265 | RNA uridylyltransferase activity | 4 | 12 |
GO:0070569 | uridylyltransferase activity | 5 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0004652 | obsolete polynucleotide adenylyltransferase activity | 6 | 3 |
GO:0004810 | CCA tRNA nucleotidyltransferase activity | 8 | 3 |
GO:0052929 | ATP:3'-cytidine-cytidine-tRNA adenylyltransferase activity | 9 | 3 |
GO:0070566 | adenylyltransferase activity | 5 | 3 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 3 |
GO:1990817 | poly(A) RNA polymerase activity | 7 | 3 |
GO:0052927 | CTP:tRNA cytidylyltransferase activity | 5 | 2 |
GO:0070567 | cytidylyltransferase activity | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.247 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.360 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.359 |
CLV_PCSK_PC1ET2_1 | 301 | 303 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 416 | 420 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 44 | 48 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 501 | 505 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.330 |
DEG_APCC_DBOX_1 | 419 | 427 | PF00400 | 0.440 |
DEG_APCC_DBOX_1 | 43 | 51 | PF00400 | 0.481 |
DEG_MDM2_SWIB_1 | 452 | 459 | PF02201 | 0.492 |
DOC_CKS1_1 | 507 | 512 | PF01111 | 0.322 |
DOC_MAPK_gen_1 | 236 | 246 | PF00069 | 0.477 |
DOC_MAPK_gen_1 | 301 | 309 | PF00069 | 0.489 |
DOC_MAPK_gen_1 | 31 | 38 | PF00069 | 0.507 |
DOC_MAPK_gen_1 | 399 | 406 | PF00069 | 0.517 |
DOC_MAPK_gen_1 | 497 | 504 | PF00069 | 0.470 |
DOC_MAPK_MEF2A_6 | 110 | 118 | PF00069 | 0.538 |
DOC_MAPK_MEF2A_6 | 331 | 338 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 420 | 429 | PF00069 | 0.406 |
DOC_MAPK_MEF2A_6 | 497 | 504 | PF00069 | 0.472 |
DOC_MAPK_NFAT4_5 | 497 | 505 | PF00069 | 0.460 |
DOC_MAPK_RevD_3 | 266 | 280 | PF00069 | 0.578 |
DOC_PP1_RVXF_1 | 195 | 202 | PF00149 | 0.322 |
DOC_PP2B_LxvP_1 | 339 | 342 | PF13499 | 0.322 |
DOC_PP2B_LxvP_1 | 363 | 366 | PF13499 | 0.384 |
DOC_PP2B_LxvP_1 | 471 | 474 | PF13499 | 0.529 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.300 |
DOC_USP7_UBL2_3 | 239 | 243 | PF12436 | 0.492 |
DOC_USP7_UBL2_3 | 401 | 405 | PF12436 | 0.204 |
DOC_USP7_UBL2_3 | 478 | 482 | PF12436 | 0.510 |
DOC_USP7_UBL2_3 | 497 | 501 | PF12436 | 0.454 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.320 |
DOC_WW_Pin1_4 | 506 | 511 | PF00397 | 0.519 |
LIG_14-3-3_CanoR_1 | 185 | 189 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 308 | 315 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 399 | 404 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 76 | 82 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 87 | 92 | PF00244 | 0.456 |
LIG_Actin_WH2_2 | 17 | 35 | PF00022 | 0.473 |
LIG_Actin_WH2_2 | 488 | 503 | PF00022 | 0.511 |
LIG_APCC_ABBA_1 | 293 | 298 | PF00400 | 0.522 |
LIG_Clathr_ClatBox_1 | 5 | 9 | PF01394 | 0.528 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.495 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.454 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.446 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.431 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.328 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.472 |
LIG_FHA_1 | 491 | 497 | PF00498 | 0.424 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.515 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.444 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.467 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.243 |
LIG_FHA_2 | 507 | 513 | PF00498 | 0.507 |
LIG_LIR_Gen_1 | 117 | 126 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 18 | 28 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 240 | 248 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 378 | 388 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 453 | 464 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 117 | 121 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 18 | 23 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 378 | 383 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 453 | 459 | PF02991 | 0.437 |
LIG_OCRL_FandH_1 | 154 | 166 | PF00620 | 0.515 |
LIG_Pex14_2 | 452 | 456 | PF04695 | 0.496 |
LIG_REV1ctd_RIR_1 | 341 | 349 | PF16727 | 0.511 |
LIG_SH2_CRK | 484 | 488 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.468 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.460 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.489 |
LIG_SH3_3 | 309 | 315 | PF00018 | 0.443 |
LIG_SH3_3 | 500 | 506 | PF00018 | 0.465 |
LIG_SUMO_SIM_anti_2 | 221 | 229 | PF11976 | 0.479 |
LIG_SUMO_SIM_anti_2 | 90 | 95 | PF11976 | 0.440 |
LIG_SUMO_SIM_par_1 | 265 | 270 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 461 | 467 | PF11976 | 0.491 |
LIG_TYR_ITIM | 428 | 433 | PF00017 | 0.441 |
LIG_UBA3_1 | 224 | 231 | PF00899 | 0.402 |
LIG_UBA3_1 | 495 | 501 | PF00899 | 0.473 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.428 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.493 |
MOD_CK2_1 | 165 | 171 | PF00069 | 0.468 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.484 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.433 |
MOD_Cter_Amidation | 277 | 280 | PF01082 | 0.627 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.429 |
MOD_GlcNHglycan | 434 | 438 | PF01048 | 0.468 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.434 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.478 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.410 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.497 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.489 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.486 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.474 |
MOD_N-GLC_1 | 208 | 213 | PF02516 | 0.421 |
MOD_N-GLC_1 | 450 | 455 | PF02516 | 0.315 |
MOD_N-GLC_2 | 357 | 359 | PF02516 | 0.475 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.343 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.424 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.387 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.475 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.340 |
MOD_NEK2_2 | 15 | 20 | PF00069 | 0.416 |
MOD_NEK2_2 | 394 | 399 | PF00069 | 0.547 |
MOD_PKA_2 | 184 | 190 | PF00069 | 0.418 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.488 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.498 |
MOD_Plk_1 | 147 | 153 | PF00069 | 0.457 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.420 |
MOD_Plk_1 | 220 | 226 | PF00069 | 0.423 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.524 |
MOD_Plk_2-3 | 347 | 353 | PF00069 | 0.263 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.458 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.449 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.378 |
MOD_Plk_4 | 267 | 273 | PF00069 | 0.473 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.472 |
MOD_Plk_4 | 399 | 405 | PF00069 | 0.305 |
MOD_Plk_4 | 491 | 497 | PF00069 | 0.492 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.467 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.311 |
MOD_ProDKin_1 | 506 | 512 | PF00069 | 0.519 |
TRG_DiLeu_BaEn_1 | 435 | 440 | PF01217 | 0.371 |
TRG_DiLeu_BaEn_1 | 461 | 466 | PF01217 | 0.500 |
TRG_DiLeu_BaLyEn_6 | 191 | 196 | PF01217 | 0.367 |
TRG_DiLeu_BaLyEn_6 | 372 | 377 | PF01217 | 0.468 |
TRG_ENDOCYTIC_2 | 380 | 383 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 430 | 433 | PF00928 | 0.363 |
TRG_ER_diArg_1 | 173 | 176 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 373 | 375 | PF00400 | 0.377 |
TRG_NES_CRM1_1 | 285 | 298 | PF08389 | 0.472 |
TRG_Pf-PMV_PEXEL_1 | 374 | 378 | PF00026 | 0.474 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUG7 | Leptomonas seymouri | 68% | 99% |
A0A0S4JS32 | Bodo saltans | 33% | 100% |
A0A0S4JSB5 | Bodo saltans | 46% | 100% |
A0A1X0NL45 | Trypanosomatidae | 47% | 99% |
A0A3S7WNX9 | Leishmania donovani | 93% | 100% |
A0A422NNU3 | Trypanosoma rangeli | 47% | 100% |
A0KPN1 | Aeromonas hydrophila subsp. hydrophila (strain ATCC 7966 / DSM 30187 / BCRC 13018 / CCUG 14551 / JCM 1027 / KCTC 2358 / NCIMB 9240 / NCTC 8049) | 25% | 100% |
A1AFX8 | Escherichia coli O1:K1 / APEC | 24% | 100% |
A4H434 | Leishmania braziliensis | 84% | 100% |
A4HSB8 | Leishmania infantum | 94% | 100% |
A4SIG1 | Aeromonas salmonicida (strain A449) | 25% | 100% |
A5UCK0 | Haemophilus influenzae (strain PittEE) | 25% | 100% |
A5UJ23 | Haemophilus influenzae (strain PittGG) | 25% | 100% |
A7ZRT7 | Escherichia coli O139:H28 (strain E24377A / ETEC) | 25% | 100% |
A8A4L0 | Escherichia coli O9:H4 (strain HS) | 24% | 100% |
A8APT7 | Citrobacter koseri (strain ATCC BAA-895 / CDC 4225-83 / SGSC4696) | 24% | 100% |
A9MPV9 | Salmonella arizonae (strain ATCC BAA-731 / CDC346-86 / RSK2980) | 25% | 100% |
A9N5Y2 | Salmonella paratyphi B (strain ATCC BAA-1250 / SPB7) | 25% | 100% |
B1IRR0 | Escherichia coli (strain ATCC 8739 / DSM 1576 / NBRC 3972 / NCIMB 8545 / WDCM 00012 / Crooks) | 24% | 100% |
B1LF48 | Escherichia coli (strain SMS-3-5 / SECEC) | 24% | 100% |
B1XG61 | Escherichia coli (strain K12 / DH10B) | 24% | 100% |
B2U1G0 | Shigella boydii serotype 18 (strain CDC 3083-94 / BS512) | 25% | 100% |
B4T674 | Salmonella newport (strain SL254) | 25% | 100% |
B4TI55 | Salmonella heidelberg (strain SL476) | 25% | 100% |
B4TVT8 | Salmonella schwarzengrund (strain CVM19633) | 25% | 100% |
B5BG15 | Salmonella paratyphi A (strain AKU_12601) | 24% | 100% |
B5F6A0 | Salmonella agona (strain SL483) | 25% | 100% |
B5FHT9 | Salmonella dublin (strain CT_02021853) | 25% | 100% |
B5QZ40 | Salmonella enteritidis PT4 (strain P125109) | 25% | 100% |
B5REG2 | Salmonella gallinarum (strain 287/91 / NCTC 13346) | 25% | 100% |
B5YR96 | Escherichia coli O157:H7 (strain EC4115 / EHEC) | 25% | 100% |
B6I427 | Escherichia coli (strain SE11) | 24% | 100% |
B7LGZ2 | Escherichia coli (strain 55989 / EAEC) | 25% | 100% |
B7LQD4 | Escherichia fergusonii (strain ATCC 35469 / DSM 13698 / CCUG 18766 / IAM 14443 / JCM 21226 / LMG 7866 / NBRC 102419 / NCTC 12128 / CDC 0568-73) | 24% | 100% |
B7LZK6 | Escherichia coli O8 (strain IAI1) | 25% | 100% |
B7MAD3 | Escherichia coli O45:K1 (strain S88 / ExPEC) | 24% | 100% |
B7N0K6 | Escherichia coli O81 (strain ED1a) | 24% | 100% |
B7ND45 | Escherichia coli O17:K52:H18 (strain UMN026 / ExPEC) | 24% | 100% |
B7NJR9 | Escherichia coli O7:K1 (strain IAI39 / ExPEC) | 24% | 100% |
B7UIW4 | Escherichia coli O127:H6 (strain E2348/69 / EPEC) | 25% | 100% |
C0PYX7 | Salmonella paratyphi C (strain RKS4594) | 25% | 100% |
C1DAG2 | Laribacter hongkongensis (strain HLHK9) | 28% | 100% |
C4ZQX3 | Escherichia coli (strain K12 / MC4100 / BW2952) | 24% | 100% |
C9ZYB2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 99% |
O97001 | Leishmania major | 94% | 100% |
P06961 | Escherichia coli (strain K12) | 24% | 100% |
P45269 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 25% | 100% |
Q0T0K7 | Shigella flexneri serotype 5b (strain 8401) | 25% | 100% |
Q0TD50 | Escherichia coli O6:K15:H31 (strain 536 / UPEC) | 24% | 100% |
Q1R6S5 | Escherichia coli (strain UTI89 / UPEC) | 24% | 100% |
Q31WX9 | Shigella boydii serotype 4 (strain Sb227) | 25% | 100% |
Q32BQ8 | Shigella dysenteriae serotype 1 (strain Sd197) | 25% | 100% |
Q3YXI6 | Shigella sonnei (strain Ss046) | 25% | 100% |
Q57JQ5 | Salmonella choleraesuis (strain SC-B67) | 25% | 100% |
Q5P3T0 | Aromatoleum aromaticum (strain EbN1) | 25% | 100% |
Q5PC82 | Salmonella paratyphi A (strain ATCC 9150 / SARB42) | 24% | 100% |
Q821A6 | Shigella flexneri | 25% | 100% |
Q8CXX6 | Escherichia coli O6:H1 (strain CFT073 / ATCC 700928 / UPEC) | 24% | 100% |
Q8XBL4 | Escherichia coli O157:H7 | 25% | 100% |
Q8Z3M9 | Salmonella typhi | 27% | 100% |
Q8ZLY4 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 25% | 100% |
V5BI79 | Trypanosoma cruzi | 47% | 99% |