Alignments for a candidate for glyA in Dechlorosoma suillum PS

GapMind for Amino acid biosynthesis

Alignments for a candidate for glyA in Dechlorosoma suillum PS

Align serine hydroxymethyltransferase subunit (EC 2.1.2.1) (characterized)
to candidate Dsui_2254 Dsui_2254 glycine/serine hydroxymethyltransferase

Query= metacyc::MONOMER-4244
         (434 letters)



>FitnessBrowser__PS:Dsui_2254
          Length = 433

 Score =  542 bits (1397), Expect = e-159
 Identities = 272/409 (66%), Positives = 322/409 (78%)

Query: 24  DPDIFSAIQKEFGRQQHEIELIASENIVSQAVLDAAGSVLTNKYAEGYPGKRYYGGCQYV 83
           DP+    +  E+ RQ+H IELIASENIVS+AVL+  GSVLTNKYAEGYPG+RYYGGC  V
Sbjct: 23  DPEAARYVAAEYARQRHSIELIASENIVSRAVLEMQGSVLTNKYAEGYPGRRYYGGCGPV 82

Query: 84  DIVEDIAIDRAKKLFNCEFANVQPNSGSQANQGVFNALAQPGDTILGLSLAAGGHLTHGA 143
           D VE +AI RAK LF C +ANVQP+SGSQANQ V+ AL QPGDTILGL LAAGGHLTHGA
Sbjct: 83  DGVEALAIARAKGLFGCAYANVQPHSGSQANQAVYLALLQPGDTILGLGLAAGGHLTHGA 142

Query: 144 PVNQSGKWFKAVHYMVKPDSHLIDMDEVRKLAQEHKPRIIIAGGSAYPRKIDFAAFRAIA 203
           P+NQSGKWF+ V Y V+ D H IDM +V +LA E++P++IIAGGSAY R +DFA FR IA
Sbjct: 143 PMNQSGKWFRGVAYGVRADDHRIDMAQVEQLAYEYRPKLIIAGGSAYSRILDFAEFRRIA 202

Query: 204 DEVGAIFLVDMAHFAGLVAAGLIPSPFPHAHVVTTTTHKTLRGPRGGMILTNDADIAKKI 263
           D VGA  LVDMAHFAGLVA G  PSP P+A VVT+TTHKTLRGPRGG+IL+NDA + K I
Sbjct: 203 DRVGARLLVDMAHFAGLVAGGAHPSPLPYADVVTSTTHKTLRGPRGGLILSNDAALGKAI 262

Query: 264 NSAIFPGIQGGPLMHVIAGKAVAFGEALRPDFKVYIKQVMDNARALGEVLVQNGFALVSG 323
           +SA+FPG+QGGPLMHVI  KAVAFGEAL+P+F+ Y  +V++NA+AL + L   G  +VSG
Sbjct: 263 DSAVFPGLQGGPLMHVIGAKAVAFGEALQPEFRSYAARVVENAQALADALAAGGLRIVSG 322

Query: 324 GTDTHLVLVDLRPKKLTGTKAEKALGRANITCNKNGIPFDPEKPMVTSGIRLGSPAGTTR 383
           GTDTHL + DLRP  LTG  AEKAL R  IT NKN IP DP+KPMVTSGIR+GSPAGT+R
Sbjct: 323 GTDTHLAVADLRPLNLTGNVAEKALERVGITLNKNAIPHDPQKPMVTSGIRVGSPAGTSR 382

Query: 384 GFGVAEFQEIGRLISEVLDGVAKNGEDGNGAVEAAVKAKAIALCDRFPI 432
           GF  AEF+ IG LI  +L+ +A N E  + AV AAV+A+   LC RFP+
Sbjct: 383 GFRTAEFRLIGGLIVHLLEALAANPEAPDPAVAAAVRAQVAELCRRFPL 431


Lambda     K      H
   0.319    0.136    0.396 

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: 621
Number of extensions: 21
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: 434
Length of database: 433
Length adjustment: 32
Effective length of query: 402
Effective length of database: 401
Effective search space:   161202
Effective search space used:   161202
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: 51 (24.3 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Apr 09 2024.

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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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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:

the paper from 2019 on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer
changes to Amino acid biosynthesis since the publication.

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

GapMind for Amino acid biosynthesis