GapMind for Amino acid biosynthesis

 

Alignments for a candidate for glyA in Paraburkholderia bryophila 376MFSha3.1

Align Serine hydroxymethyltransferase 2; SHMT 2; Serine methylase 2; EC 2.1.2.1 (characterized)
to candidate H281DRAFT_00990 H281DRAFT_00990 serine hydroxymethyltransferase (EC 2.1.2.1)

Query= SwissProt::Q3JGP5
         (424 letters)



>FitnessBrowser__Burk376:H281DRAFT_00990
          Length = 431

 Score =  631 bits (1628), Expect = 0.0
 Identities = 312/418 (74%), Positives = 351/418 (83%)

Query: 7   FFSQSLAERDASVRGAILKELERQQSQVELIASENIVSRAVLDAQGSVLTNKYAEGYPGK 66
           FF++ L  RD  +   I  EL RQQ+Q+ELIASENIVS AV++AQG+VLTNKYAEGYP K
Sbjct: 7   FFAEPLQSRDPVIASEIALELRRQQTQIELIASENIVSAAVMEAQGTVLTNKYAEGYPSK 66

Query: 67  RYYGGCEFADEVEALAIERVKRLFNAGHANVQPHSGAQANGAVMLALAKPGDTVLGMSLD 126
           RYYGGCE  D VEALAI+RVK LF A  ANVQPHSGAQANGAVMLAL KPG+TV+GMSLD
Sbjct: 67  RYYGGCEHVDRVEALAIDRVKALFEAEFANVQPHSGAQANGAVMLALVKPGETVMGMSLD 126

Query: 127 AGGHLTHGAKPALSGKWFNALQYGVSRDTMLIDYDQVEALAQQHKPSLIIAGFSAYPRKL 186
           AGGHLTHGA+PALSGKWFNA+QYGV+  T  +DY+QV +LAQ+H+P LIIAG+SAYPR L
Sbjct: 127 AGGHLTHGARPALSGKWFNAVQYGVNPQTYRVDYEQVRSLAQEHRPKLIIAGYSAYPRAL 186

Query: 187 DFARFRAIADSVGAKLMVDMAHIAGVIAAGRHANPVEHAHVVTSTTHKTLRGPRGGFVLT 246
           DFA FR IADSVGA LMVDMAHIAG++AAGRH NPV  A VVTSTTHKTLRGPRGGF+LT
Sbjct: 187 DFAAFRDIADSVGALLMVDMAHIAGIVAAGRHENPVRFADVVTSTTHKTLRGPRGGFILT 246

Query: 247 NDEEIAKKINSAVFPGLQGGPLMHVIAGKAVAFGEALTDDFKTYIDRVLANAQALGDVLK 306
           N+ +IAKKINSAVFPGLQGGPLMHVIAGKAVAFGEAL  +F  YID+VL NAQALGDVLK
Sbjct: 247 NNGDIAKKINSAVFPGLQGGPLMHVIAGKAVAFGEALRPEFTAYIDQVLRNAQALGDVLK 306

Query: 307 AGGVDLVTGGTDNHLLLVDLRPKGLKGAQVEQALERAGITCNKNGIPFDPEKPTITSGIR 366
           +GG+ LVT GTDNHLLLVDLR K L G Q E+ALERAGITCNKNGIPFD E PT+TSGIR
Sbjct: 307 SGGLSLVTDGTDNHLLLVDLRSKRLTGTQAEKALERAGITCNKNGIPFDTESPTVTSGIR 366

Query: 367 LGTPAGTTRGFGAAEFREVGRLILEVFEALRTNPEGDHATEQRVRREIFALCERFPIY 424
           LGTPAGTTRGFG A+F ++G++ILEV  AL   P GD   E+ VR  +  LC +FPIY
Sbjct: 367 LGTPAGTTRGFGTAQFEQIGQMILEVLSALEQEPAGDEQVERAVRSRVRDLCSQFPIY 424


Lambda     K      H
   0.318    0.136    0.391 

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: 660
Number of extensions: 24
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: 424
Length of database: 431
Length adjustment: 32
Effective length of query: 392
Effective length of database: 399
Effective search space:   156408
Effective search space used:   156408
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:

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