GapMind for Amino acid biosynthesis

 

Alignments for a candidate for glyA in Desulfarculus baarsii DSM 2075

Align Serine hydroxymethyltransferase; SHMT; Serine methylase; L-threonine/L-allo-threonine aldolase; EC 2.1.2.1; EC 4.1.2.48 (characterized)
to candidate WP_013259861.1 DEBA_RS15345 serine hydroxymethyltransferase

Query= SwissProt::D3DKC4
         (427 letters)



>NCBI__GCF_000143965.1:WP_013259861.1
          Length = 413

 Score =  442 bits (1137), Expect = e-129
 Identities = 220/408 (53%), Positives = 289/408 (70%)

Query: 1   MRHLFNTDAEIYEAIVKEYERQFYHLELIASENFTSLAVMEAQGSVMTNKYAEGLPHKRY 60
           M  L  TD++I E I +E  RQ   L +I SEN+ S AV+ A GS++ NKY+EG P KRY
Sbjct: 1   MDQLRETDSQIAELIQREAARQANVLRMIPSENYASAAVLTATGSILANKYSEGYPRKRY 60

Query: 61  YGGCEFVDIAEDLAIERAKALFDAEHANVQPHSGTQANMAVYMAVLKPGDTIMGMDLSHG 120
           Y G EF+D  E++A++RA+ALF AEHANVQP+SG+ ANMAVY+ +L     +MGMDL+ G
Sbjct: 61  YQGQEFIDQIEEVAVQRARALFGAEHANVQPYSGSPANMAVYLGLLGAEGRVMGMDLAAG 120

Query: 121 GHLTHGAKVNFSGKIYNAVYYGVHPETHLIDYDQLYRLAKEHKPKLIVGGASAYPRVIDW 180
           GHLTHGAKV+FSG  Y+   YG+  E  LIDY+   RLA+E +P+LI  GAS+YPR+ID+
Sbjct: 121 GHLTHGAKVSFSGSYYDVRQYGLSRENGLIDYEAARRLAREFRPQLIFCGASSYPRIIDF 180

Query: 181 AKLREIADSVGAYLMVDMAHYAGLIAGGVYPNPVPYAHFVTSTTHKTLRGPRSGFILCKK 240
           A   EIA  VGA+L  D++H +GL   G++P+P+P+A  +T+TTHK LRGPR G ILC+ 
Sbjct: 181 AIFGEIAREVGAFLAADISHISGLCVTGLHPHPLPHADVITTTTHKMLRGPRGGMILCRA 240

Query: 241 EFAKDIDKSVFPGIQGGPLMHVIAAKAVAFKEAMSQEFKEYARQVVANARVLAEEFIKEG 300
             A  IDK+VFPG+QGGP  HV AA AVA KEA    F EY RQ+VANA+ LA+E +  G
Sbjct: 241 GLAPAIDKAVFPGLQGGPHNHVTAAIAVALKEASGTAFVEYCRQIVANAKALADELMARG 300

Query: 301 FKVVSGGTDSHIVLLDLRDTGLTGREVEEALGKANITVNKNAVPFDPLPPVKTSGIRLGT 360
           FK+++GGTD+H+ L+D    GLTG+ + +A+ KA I  N N +PFDP      SG+RLGT
Sbjct: 301 FKLITGGTDNHLALIDASCRGLTGKILAQAMEKAGIVANANKIPFDPRSANDPSGVRLGT 360

Query: 361 PAMTTRGMKEDQMRIIARLISKVIKNIGDEKVIEYVRQEVIEMCEQFP 408
           PA+T+RGMKE +MR +A LI +V   +GDE  +  +R EV EMC  FP
Sbjct: 361 PALTSRGMKEPEMRRVAALIDRVTDVVGDEAALAKIRAEVEEMCAAFP 408


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: 560
Number of extensions: 18
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: 413
Length adjustment: 32
Effective length of query: 395
Effective length of database: 381
Effective search space:   150495
Effective search space used:   150495
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: 50 (23.9 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:

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