GapMind for catabolism of small carbon sources

 

Alignments for a candidate for catB in Marivita geojedonensis DPG-138

Align muconate cycloisomerase (EC 5.5.1.1) (characterized)
to candidate WP_085635323.1 MGEO_RS03455 muconate cycloisomerase

Query= metacyc::MONOMER-14643
         (382 letters)



>NCBI__GCF_002115805.1:WP_085635323.1
          Length = 387

 Score =  388 bits (997), Expect = e-112
 Identities = 200/380 (52%), Positives = 270/380 (71%), Gaps = 2/380 (0%)

Query: 2   LATAIESIETIIVDLPTIRPHKLAMHTMQNQTLVIIRVRCADGIEGIGESTTIGGLAYGN 61
           L T I+ IET+I+D+PTIR H L+M TM+ QT V++ VR +DG EGIGE TTIGGL+YG 
Sbjct: 5   LVTKIDQIETMILDIPTIRGHVLSMATMRTQTAVVVVVRFSDGSEGIGEGTTIGGLSYGP 64

Query: 62  ESPDSIKTNIDKHFAPLLIGQDSGNVNAAMLRLERSIRGNTFAKSGIETALLDAHGKRLG 121
           ESP+ IK+ ID + AP LIG+D+ +VNAA+  +++ ++GN  AK+ +E AL D  GKRLG
Sbjct: 65  ESPEGIKSAIDTYIAPALIGRDADSVNAAVHLIDKLVKGNRIAKTAVEIALWDGLGKRLG 124

Query: 122 LPVSELLGGRVRDALPVAWTLASGDTEKDIAEAEKMLDLRRHRIFKLKIGAGEVNRDLAH 181
           + V++L GG V + LPVAWTLASG++E DIAEA +M++ RRH IFKLKIG   V  D+AH
Sbjct: 125 VSVAQLFGGAVHERLPVAWTLASGNSETDIAEAHEMIETRRHNIFKLKIGKRSVRDDVAH 184

Query: 182 VIAIKKALGDRASVRVDVNQAWDEAVALRACRILGTNGIDLVEQPISRNNRGGMARLNAM 241
           V  IK+A+GD ASVRVDVN AW    A    + L   G +LVEQP+    R  MA L++ 
Sbjct: 185 VARIKQAVGDAASVRVDVNTAWSLQDARWGLKGLQDAGCELVEQPVPARYRRAMAELSSG 244

Query: 242 SPAPIMADESIECVEDAFNLAREGAASVFALKIAKNGGPRAVLRTASIAEAAGIALYGGT 301
               +MADE++   EDA  +    AA VFA+K+A++GG +      +I +AAG+ LYGGT
Sbjct: 245 YEIAVMADEALNGPEDALAVVSANAADVFAVKVAQSGGLKRASEVIAIGQAAGLGLYGGT 304

Query: 302 MLEGGLGTMASAHAFVTLNKLAWDTELFGPLLLTEDILSEPLVYRDFELHVPNTPGLGLS 361
           MLE GLGT A+   F T   L+W TELFGPLLLT++IL++P+VYRDF + +P   G+G++
Sbjct: 305 MLETGLGTAAALQLFATTEHLSWGTELFGPLLLTDEILAKPIVYRDFCVEIPKGVGIGVT 364

Query: 362 LDEERLAFFRRD--KTSTAI 379
           LD +++AFFRRD  +T TA+
Sbjct: 365 LDPDKIAFFRRDVGRTITAV 384


Lambda     K      H
   0.319    0.136    0.386 

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: 346
Number of extensions: 10
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: 382
Length of database: 387
Length adjustment: 30
Effective length of query: 352
Effective length of database: 357
Effective search space:   125664
Effective search space used:   125664
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 (21.7 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