GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gyaR in Methylocystis bryophila S285

Align Glyoxylate reductase; EC 1.1.1.26 (characterized)
to candidate WP_085773692.1 B1812_RS12475 D-glycerate dehydrogenase

Query= SwissProt::Q9C4M5
         (331 letters)



>NCBI__GCF_002117405.1:WP_085773692.1
          Length = 331

 Score =  267 bits (683), Expect = 2e-76
 Identities = 149/331 (45%), Positives = 205/331 (61%), Gaps = 10/331 (3%)

Query: 2   KPKVFITRQIPENGIKMIEKFYEIELWKDPKAPPRGVLLEKVREVDALVTLVTDKVDKEL 61
           KP V +TR++PE     + + ++  L ++ K P    L E +R  D LV  +TD++D  L
Sbjct: 5   KPVVVVTRRLPEVIETRMRELFDARLNENDKPPTHEELAEAMRTADVLVPTITDRIDASL 64

Query: 62  LENA-PKLKIIAQYAVGYDNIDIEEATKRGIYVTNTPGVLTDATADLAFALLLAVARRIV 120
           +  A  ++K+IA +  G DNID+  A +R I VTNTPGVLT+ TAD+  AL+LAVARRIV
Sbjct: 65  IAQAGEQMKLIANFGNGVDNIDVASALRRSITVTNTPGVLTEDTADMTMALILAVARRIV 124

Query: 121 EADAFVRSGEWKKSEVGWHPLMFLGYGLKGKTLGIVGFGRIGQALAKRAKGFGMKIIYYS 180
           E    + +G W     GW P   LG  + GK LGIVG GRIGQALA+RA  FG+ I Y++
Sbjct: 125 EGANVIGAGSWG----GWSPTWMLGRRITGKRLGIVGMGRIGQALARRANAFGLSIHYHN 180

Query: 181 RTRKP-EAEEEIGAEYVD-FETLLKESDFISLHVPLTKETYHMIGEKELKLMKPNAILIN 238
           R R P E EE++ A Y +  + +L   D +S+H P T  TYH++  + LK ++P+AIL+N
Sbjct: 181 RRRLPAEIEEQLEATYWESLDQMLARVDILSIHCPHTPATYHLLSARRLKQLRPHAILVN 240

Query: 239 TSRGAVVDTNALIKALKEGWIAGAGLDVFEEEPYYNEELFKLK---NVVLAPHIGSATHE 295
           T+RG +VD N L++ L+   +AGAGLDVFE EP  + +L KL     V L PH+GSAT E
Sbjct: 241 TARGEIVDENELVRMLESDELAGAGLDVFEHEPAVSPKLLKLAQAGKVTLLPHMGSATIE 300

Query: 296 AREGMAELVAKNLIAFAKGEIPPNLVNKDVL 326
            R  M E V  N+  F  G  PP+ V   +L
Sbjct: 301 GRIDMGEKVIVNIKTFIDGHRPPDRVLPSML 331


Lambda     K      H
   0.317    0.137    0.392 

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: 266
Number of extensions: 16
Number of successful extensions: 5
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: 331
Length of database: 331
Length adjustment: 28
Effective length of query: 303
Effective length of database: 303
Effective search space:    91809
Effective search space used:    91809
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 09 2024. 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