GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ltaE in Desulfacinum infernum DSM 9756

Align Serine hydroxymethyltransferase; SHMT; Serine methylase; EC 2.1.2.1; L-threonine/L-allo-threonine aldolase; EC 4.1.2.48 (uncharacterized)
to candidate WP_073042231.1 BUB04_RS18410 serine hydroxymethyltransferase

Query= curated2:D3DKC4
         (427 letters)



>NCBI__GCF_900129305.1:WP_073042231.1
          Length = 425

 Score =  523 bits (1346), Expect = e-153
 Identities = 259/407 (63%), Positives = 316/407 (77%)

Query: 4   LFNTDAEIYEAIVKEYERQFYHLELIASENFTSLAVMEAQGSVMTNKYAEGLPHKRYYGG 63
           L + D EI + +  E  RQ   LELIASENF S AV  AQGSV+TNKYAEG P +RYYGG
Sbjct: 6   LQSMDPEIAQVLRDEEHRQRSKLELIASENFVSDAVRIAQGSVLTNKYAEGYPGRRYYGG 65

Query: 64  CEFVDIAEDLAIERAKALFDAEHANVQPHSGTQANMAVYMAVLKPGDTIMGMDLSHGGHL 123
           CEFVD+AE LA ERA  LF AE+ANVQPHSG+QANMAVY A+L+PGDTIMGMDL  GGHL
Sbjct: 66  CEFVDVAERLAQERACRLFGAEYANVQPHSGSQANMAVYFALLEPGDTIMGMDLRQGGHL 125

Query: 124 THGAKVNFSGKIYNAVYYGVHPETHLIDYDQLYRLAKEHKPKLIVGGASAYPRVIDWAKL 183
           THG+ V+FSG+++  V YGV P+T  ID+D L RLA+EH+P+LIV GASAYPRVID+A+ 
Sbjct: 126 THGSPVSFSGRLFKVVSYGVKPDTETIDFDGLARLAREHRPRLIVAGASAYPRVIDFARF 185

Query: 184 REIADSVGAYLMVDMAHYAGLIAGGVYPNPVPYAHFVTSTTHKTLRGPRSGFILCKKEFA 243
           REI D VGAYLMVDMAH AGLI+ G++PNPVP+AH VTSTTHKTLRGPR G IL   E  
Sbjct: 186 REICDEVGAYLMVDMAHIAGLISAGLHPNPVPHAHVVTSTTHKTLRGPRGGLILAGAELG 245

Query: 244 KDIDKSVFPGIQGGPLMHVIAAKAVAFKEAMSQEFKEYARQVVANARVLAEEFIKEGFKV 303
           + +D  +FPGIQGGPLMHVIAAKAVAF+EAM   FKEY R++V NAR LAE  +  G+++
Sbjct: 246 RKLDSQIFPGIQGGPLMHVIAAKAVAFQEAMQPCFKEYQRRIVQNARTLAEALLSHGYRL 305

Query: 304 VSGGTDSHIVLLDLRDTGLTGREVEEALGKANITVNKNAVPFDPLPPVKTSGIRLGTPAM 363
           VSGGTD+H++L+DLR+ GLTG++ EEAL KA ITVNKN++PFDP  P  TSGIR+GT A+
Sbjct: 306 VSGGTDNHMMLVDLRNKGLTGKQAEEALDKAGITVNKNSIPFDPQTPHVTSGIRIGTAAV 365

Query: 364 TTRGMKEDQMRIIARLISKVIKNIGDEKVIEYVRQEVIEMCEQFPLY 410
           TTRGM+   M  IAR I + +  + D + +  ++ +V   CE FPL+
Sbjct: 366 TTRGMEPSHMVEIARFIHQALSAVDDSQRLAVLKADVAAFCESFPLH 412


Lambda     K      H
   0.319    0.136    0.395 

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: 617
Number of extensions: 26
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: 427
Length of database: 425
Length adjustment: 32
Effective length of query: 395
Effective length of database: 393
Effective search space:   155235
Effective search space used:   155235
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 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