GapMind for Amino acid biosynthesis

 

Alignments for a candidate for tpiA in Shewanella loihica PV-4

Align triose-phosphate isomerase (EC 5.3.1.1) (characterized)
to candidate 5208242 Shew_0754 phosphoglycerate kinase (RefSeq)

Query= BRENDA::P36204
         (654 letters)



>FitnessBrowser__PV4:5208242
          Length = 391

 Score =  331 bits (849), Expect = 3e-95
 Identities = 183/391 (46%), Positives = 255/391 (65%), Gaps = 12/391 (3%)

Query: 9   VDLKGKRVIMRVDFNVPVKDGVVQDDTRIRAALPTIKYALEQGAKVILLSHLGRP-KGEP 67
           +DL+GKRV++R D NVPV +GVV  D R+RA+LPTIK ALE+GA V+++SHLGRP +GE 
Sbjct: 9   LDLQGKRVLIREDLNVPVSNGVVTSDARLRASLPTIKLALEKGAAVMVMSHLGRPTEGEY 68

Query: 68  SPEFSLAPVAKRLSELLGKEVKFVPAVVGDEVKKAVEELKEGEVLLLENTRFHPGETKND 127
           + EFS+ PV   L + L   V+     + D V+  V     GEV++ EN RF+ GE KND
Sbjct: 69  NSEFSMQPVVDYLEKALDCPVRLAKDYL-DGVEANV-----GEVVVFENVRFNVGEKKND 122

Query: 128 PELAKFWASLADIHVNDAFGTAHRAHASNVGIAQFIP-SVAGFLMEKEIKFLSKVTYNPE 186
             LAK  A+L D++V DAFGTAHRA AS  G+  + P + AG L+  E++ L K   NP 
Sbjct: 123 EALAKKLAALCDVYVMDAFGTAHRAQASTHGVGLYAPVACAGPLLAGELEALGKAMDNPA 182

Query: 187 KPYVVVLGGAKVSDKIGVITNLMEKADRILIGGAMMFTFLKALGKEVGSSRVEEDKIDLA 246
           +P V ++GG+KVS K+ V+ +L    D++++GG +  TF+ A G  VG S  E D ID A
Sbjct: 183 RPLVAIVGGSKVSTKLTVLESLSGIVDQLVVGGGIANTFIAAAGHNVGKSLYEADLIDEA 242

Query: 247 KELLEKAKEKGVEIVLPVDAVIAQKIEPGVEKKVVRIDDGIPEGWMGLDIGPETIELFKQ 306
           K L+  A+ +G +I +P D V+A +  P     +  +D    E  M  DIGP++ E   +
Sbjct: 243 KRLVANAQSRGGDIPVPTDVVVASEFSPTASATLKAVDQVADED-MIFDIGPDSAEALAE 301

Query: 307 KLSDAKTVVWNGPMGVFEIDDFAEGTKQVALAIAALTEKGAITVVGGGDSAAAVNKFGLE 366
            L +A T+VWNGP+GVFE D F EGTK++A AIA   +  A ++ GGGD+ AAV+K+ + 
Sbjct: 302 ILKNAGTIVWNGPVGVFEFDQFGEGTKRIAQAIA---DSSAFSIAGGGDTLAAVDKYDIA 358

Query: 367 DKFSHVSTGGGASLEFLEGKELPGIASIADK 397
           DK S++STGGGA LEFLEGKELP +A +  +
Sbjct: 359 DKVSYISTGGGAFLEFLEGKELPAVAMLESR 389


Lambda     K      H
   0.317    0.137    0.386 

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: 589
Number of extensions: 34
Number of successful extensions: 6
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: 654
Length of database: 391
Length adjustment: 34
Effective length of query: 620
Effective length of database: 357
Effective search space:   221340
Effective search space used:   221340
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: 52 (24.6 bits)

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 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