Align 2-amino-5-chloromuconic acid deaminase; 2-aminomuconate deaminase; EC 3.5.99.5 (characterized)
to candidate WP_084055551.1 B9A12_RS00285 Asp-tRNA(Asn)/Glu-tRNA(Gln) amidotransferase subunit GatA
Query= SwissProt::Q38M35 (462 letters) >NCBI__GCF_900176285.1:WP_084055551.1 Length = 487 Score = 159 bits (401), Expect = 3e-43 Identities = 136/485 (28%), Positives = 224/485 (46%), Gaps = 52/485 (10%) Query: 6 LSLAEHAARLRRRELTAVALIDTCAQHHARMEPRLNAYKTWDGARARSAAAAVDTLLDQG 65 L++ E L R+E + +++ + +++P LN+Y +A A A DT Sbjct: 7 LTIHETRQVLLRKEASVTEVVNAYLERIEKLDPSLNSYLIVLADQALEEARAYDTGALPL 66 Query: 66 QDLGPLMGLPVSVKDLYGVPGLPVFAGS---DEALPEAWQAAGPLVARLQRQLGIVVGKT 122 QD PL G+P+++KD+ G+ GS ++ +P +V RL+ I +GKT Sbjct: 67 QDR-PLGGVPLALKDVLCTQGVRTTCGSRILEDFIPPY---DATVVQRLKESGAIFLGKT 122 Query: 123 HTVEFAFGGLGVNAHWGTPRNPWSPHEHRVPGGSSAGAGVSLVQGSALLALGTDTAGSVR 182 + EFA G N+ +G RNPW RVPGGSS G+ ++ ALGTDT GS+R Sbjct: 123 NMDEFAMGSSNENSAFGPTRNPWD--RQRVPGGSSGGSAAAVAAELCAGALGTDTGGSIR 180 Query: 183 VPASMTGQVGLKTTVGRWPVEGIVPLSSSLDTAGVLTRTVEDLAYAFAAL----DTESQG 238 PAS G VGLK T GR G+V +SSLD G +T+ V+D A + +S Sbjct: 181 QPASFCGVVGLKPTYGRVSRYGLVAFASSLDQIGPITKDVKDAALLLQVIAGHDPRDSTC 240 Query: 239 LPAPA-------PVRVQGLRVGVPTNHFWDDIDPSIAAAVEAAVQRLAQAGAQVVRFPLP 291 L P +QG+ +G+P +F + +DP ++ A+E A GA++V LP Sbjct: 241 LEQPVGDLLTHLDKPIQGMTLGIPKEYFVEGMDPEVSRAMEDAFSVFKDLGARLVDISLP 300 Query: 292 HCEEAFDIFRRGGLAASELAAYLDQHFPHKVERLDPVVRDRVRWAEQVSSVEY---LRRK 348 H + + + +A +E ++ L ++ K RD + + S + ++R+ Sbjct: 301 HTD--YGVAAYYIIAPAEASSNLARYDGVKYGFRKQQARDLLTMYRETRSHGFGSEVKRR 358 Query: 349 AVLQRCGAGAA---------------------RLFDDVDVLLTPTVPASPPRLADIGTVE 387 +L A + F DV++ P VP ++ + + Sbjct: 359 IMLGTYSLSAGYYDAYYRKASQVRTLIKQDFMQAFHHCDVIIAPVVPTPAFKIGE----K 414 Query: 388 TYAPANMKAMR-NTAISNLFGWCALTMPVGLDANRMPVGLQLMGPPRAEARLIGIALGIE 446 P M T ++L G +++P G ++ +PVGLQ++GP E ++ ++ E Sbjct: 415 AQDPLQMYLSDILTLPASLAGIPGISVPCGYTSDGLPVGLQVLGPHFGEPTILQVSHNFE 474 Query: 447 -ALIG 450 A IG Sbjct: 475 KATIG 479 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: 509 Number of extensions: 29 Number of successful extensions: 6 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 462 Length of database: 487 Length adjustment: 33 Effective length of query: 429 Effective length of database: 454 Effective search space: 194766 Effective search space used: 194766 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: 51 (24.3 bits)
This GapMind analysis is from Apr 09 2024. 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