GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gci in Halomonas desiderata SP1

Align D-galactarolactone cycloisomerase (EC 5.5.1.27) (characterized)
to candidate WP_086510675.1 BZY95_RS14785 mandelate racemase/muconate lactonizing enzyme family protein

Query= BRENDA::A9CEQ8
         (378 letters)



>NCBI__GCF_002151265.1:WP_086510675.1
          Length = 378

 Score =  560 bits (1443), Expect = e-164
 Identities = 271/375 (72%), Positives = 312/375 (83%)

Query: 1   MKITAVRTHLLEHRLDTPFESASMRFDRRAHVLVEIECDDGTVGWGECLGPARPNAAVVQ 60
           MKI AV TH+L+H LDT FESASM F RR H LVEI CDDGT+GWGECLGPA+PNAAVV+
Sbjct: 1   MKIAAVHTHILDHVLDTTFESASMYFARRQHCLVEIVCDDGTIGWGECLGPAQPNAAVVK 60

Query: 61  AYSGWLIGQDPRQTEKIWAVLYNALRDQGQRGLSLTALSGIDIALWDIKGKHYGASISML 120
           AY   LIGQDP QTE++W  LYN LRDQGQRGL++TALSGIDIALWDIKGK +G  IS L
Sbjct: 61  AYRAALIGQDPLQTERLWLELYNRLRDQGQRGLTVTALSGIDIALWDIKGKRFGVPISTL 120

Query: 121 LGGRWRESVRAYATGSFKRDNVDRVSDNASEMAERRAEGFHACKIKIGFGVEEDLRVIAA 180
           LGGR+R+SVRAYATGSF+R  VDRV DNA E+A  R EGFHA KIKIGFGV+EDLRVI A
Sbjct: 121 LGGRFRDSVRAYATGSFRRAGVDRVEDNAREVAGYRREGFHAVKIKIGFGVDEDLRVIEA 180

Query: 181 VREAIGPDMRLMIDANHGYTVTEAITLGDRAAGFGIDWFEEPVVPEQLDAYARVRAGQPI 240
           VRE+IGPDMRLMIDANHGY   EA+ +G RAA FGIDWFEEPV+PE + AY  VRA QPI
Sbjct: 181 VRESIGPDMRLMIDANHGYDYLEAVEVGRRAAKFGIDWFEEPVLPEHVSAYRAVRADQPI 240

Query: 241 PVAGGETWHGRYGMWQALSAGAVDILQPDLCGCGGFSEIQKIATLATLHGVRIVPHVWGT 300
           PVAGGETWHGRY M + L+  AVDI+QPD+CG GGF+EI+++A +A LHGVR+VPHVWGT
Sbjct: 241 PVAGGETWHGRYAMHEPLATRAVDIIQPDICGVGGFTEIRRVADMAALHGVRLVPHVWGT 300

Query: 301 GVQIAAALQFMAAMTPDPVRVNPIEPIMEFDRTHNPFRQAVLREPLEAVNGVVTIPDGPG 360
            V +AA+LQFMAA+ P+P R +PIEPI+EFDRT NPFRQAV+  P+E   GVV IPDGPG
Sbjct: 301 AVCLAASLQFMAALLPNPPRRDPIEPILEFDRTENPFRQAVVTTPIEHDRGVVAIPDGPG 360

Query: 361 LGIEINRDALTEFRM 375
           LGIEI+R+AL  F +
Sbjct: 361 LGIEIDREALARFAL 375


Lambda     K      H
   0.321    0.138    0.431 

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: 603
Number of extensions: 18
Number of successful extensions: 1
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: 378
Length of database: 378
Length adjustment: 30
Effective length of query: 348
Effective length of database: 348
Effective search space:   121104
Effective search space used:   121104
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 (21.9 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

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:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

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