GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gyaR in Phyllobacterium brassicacearum STM 196

Align Glyoxylate reductase; EC 1.1.1.26 (characterized)
to candidate WP_106711636.1 CU102_RS13520 D-glycerate dehydrogenase

Query= SwissProt::Q9C4M5
         (331 letters)



>NCBI__GCF_003010955.1:WP_106711636.1
          Length = 333

 Score =  252 bits (644), Expect = 8e-72
 Identities = 144/327 (44%), Positives = 202/327 (61%), Gaps = 11/327 (3%)

Query: 2   KPKVFITRQIPENGIKMIEKFYEIELWKDPKAPPRGVLLEKVREVDALVTLVTDKVDKEL 61
           KP V ITR++P+     + + +E  L  D +   +  L+E V++   LV  +TD V +E+
Sbjct: 6   KPLVVITRKLPDPIETRMRELFEARLNVDDRRLSKAELIEAVKQAHVLVPTITDHVSEEI 65

Query: 62  LENA-PKLKIIAQYAVGYDNIDIEEATKRGIYVTNTPGVLTDATADLAFALLLAVARRIV 120
           +  A P LK+IA +  G DNID+  A KRGI VTNTP VLT+ TAD+  AL+LA  RR+V
Sbjct: 66  INAAGPNLKLIANFGNGTDNIDVVAAAKRGITVTNTPNVLTEDTADMTMALMLAAPRRLV 125

Query: 121 E-ADAFVRSGEWKKSEVGWHPLMFLGYGLKGKTLGIVGFGRIGQALAKRAKGFGMKIIYY 179
           E A   +  G+W+    GW P   LG  + GK LGIVG GRIG A+A+RAK FG+ I Y+
Sbjct: 126 EGASILLDDGKWE----GWGPTWMLGRRIWGKRLGIVGMGRIGTAVARRAKAFGLSIHYH 181

Query: 180 SRTR-KPEAEEEIGAEYVD-FETLLKESDFISLHVPLTKETYHMIGEKELKLMKPNAILI 237
           +R    P+ EEE+ A Y +  + +L   D IS++ P T  T+H++  + L LM+P A ++
Sbjct: 182 NRKPVNPKTEEELEATYWESLDQMLARMDIISVNCPSTPATFHLLSARRLALMQPTAFIV 241

Query: 238 NTSRGAVVDTNALIKALKEGWIAGAGLDVFEEEPYYNEELFKLK---NVVLAPHIGSATH 294
           NT+RG ++D +ALI+ L+ G ++GA LDVFE EP  N +L KL     VV+ PH+GSAT 
Sbjct: 242 NTARGQIIDEHALIEQLERGKLSGAALDVFEHEPAVNSKLRKLAKHGKVVILPHMGSATL 301

Query: 295 EAREGMAELVAKNLIAFAKGEIPPNLV 321
           E R  M E V  N+  F  G  PP+ V
Sbjct: 302 EGRIDMGEKVIINIRTFIDGHRPPDRV 328


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: 12
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: 333
Length adjustment: 28
Effective length of query: 303
Effective length of database: 305
Effective search space:    92415
Effective search space used:    92415
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 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