Align 2-amino-5-chloromuconic acid deaminase; 2-aminomuconate deaminase; EC 3.5.99.5 (characterized)
to candidate WP_110206069.1 DNK54_RS06065 Asp-tRNA(Asn)/Glu-tRNA(Gln) amidotransferase subunit GatA
Query= SwissProt::Q38M35 (462 letters) >NCBI__GCF_003194585.1:WP_110206069.1 Length = 522 Score = 168 bits (426), Expect = 3e-46 Identities = 154/493 (31%), Positives = 221/493 (44%), Gaps = 59/493 (11%) Query: 7 SLAEHAARLRRRELTAVAL----IDTCAQHHARMEPRLNAYKTWDGARARSAAAAVDTLL 62 S AE AA L E+T+V L +D A E ++A+ D A + AAA D Sbjct: 11 SAAELAAALAAGEVTSVELTQAHLDRIAAVDGNAEAGVHAFLHVDTEGALAEAAASDARR 70 Query: 63 DQGQDLGPLMGLPVSVKDLYGVPGLPVFAGSDEALPEAWQAA-GPLVARLQRQLGI-VVG 120 G+ L L G+PV+VKD+ GLP GS + E W V R + G+ ++G Sbjct: 71 AAGEPLSELDGVPVAVKDVLTTTGLPTTCGSK--ILEGWVPPYDATVVRKLKAAGLPILG 128 Query: 121 KTHTVEFAFGGLGVNAHWGTPRNPWSPHEHRVPGGSSAGAGVSLVQGSALLALGTDTAGS 180 KT+ EFA G ++ +G RNPW+ R+PGGS G+ ++ A LALGTDT GS Sbjct: 129 KTNMDEFAMGSSTEHSAYGPTRNPWALD--RIPGGSGGGSAAAVAAYEAPLALGTDTGGS 186 Query: 181 VRVPASMTGQVGLKTTVGRWPVEGIVPLSSSLDTAGVLTRTVEDLAY------AFAALDT 234 +R P ++TG VG+K T G G+V +++SLD G +TRTV D A LD+ Sbjct: 187 IRQPGAVTGTVGVKPTYGALSRYGLVAMANSLDQVGPVTRTVLDAALLHELVGGHDPLDS 246 Query: 235 ESQGLPAPAPVR---------VQGLRVGVPTNHFWDDIDPSIAAAVEAAVQRLAQAGAQV 285 S P PA + GL+VGV + P + A AV+ L AGA+V Sbjct: 247 TSIDAPVPALAAAAREGALGDLSGLKVGVIQELAGEGYQPGVLARFNEAVELLVGAGAEV 306 Query: 286 VRFPLPH-------------CEEA-----FDIFRRG----------GLAASELAAYLDQH 317 V P CE + FD R G A + A D Sbjct: 307 VEVSCPSFVHALATYYLVMPCEASSNLAKFDAMRYGLRVLPEGVDAPSAEEVMRASRDAG 366 Query: 318 FPHKVERLDPVVRDRVRWAEQVSSVEYLRRKAVLQRCGAGAARLFDDVDVLLTPTVPASP 377 F +V+R ++ + Y + + V F VDVL++PT P + Sbjct: 367 FGDEVKR--RIILGTYALSSGYYDAYYGQAQKVRTLISRDFEAAFASVDVLVSPTAPTTA 424 Query: 378 PRLADIGTVETYAPANMKAMRNTAISNLFGWCALTMPVGL-DANRMPVGLQLMGPPRAEA 436 +L + N A T +NL G +++P GL D + +PVG Q++ P +A Sbjct: 425 FKLGEKLDDPLAMYLNDLA---TIPANLAGVPGMSLPAGLADEDGLPVGFQILAPATEDA 481 Query: 437 RLIGIALGIEALI 449 RL + +EAL+ Sbjct: 482 RLYRVGGALEALL 494 Lambda K H 0.320 0.135 0.411 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 549 Number of extensions: 27 Number of successful extensions: 6 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 462 Length of database: 522 Length adjustment: 34 Effective length of query: 428 Effective length of database: 488 Effective search space: 208864 Effective search space used: 208864 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory