GapMind for Amino acid biosynthesis

 

Alignments for a candidate for agx1 in Desulfitobacterium hafniense DCB-2

Align Alanine--glyoxylate aminotransferase 1; EC 2.6.1.44 (characterized)
to candidate WP_005815362.1 DHAF_RS24160 alanine--glyoxylate aminotransferase family protein

Query= SwissProt::P43567
         (385 letters)



>NCBI__GCF_000021925.1:WP_005815362.1
          Length = 390

 Score =  171 bits (433), Expect = 3e-47
 Identities = 116/363 (31%), Positives = 189/363 (52%), Gaps = 30/363 (8%)

Query: 6   DTLLIPGPIILSGAVQKALDVPSLGHTSPEFVSIFQRVLKNTRAVFKSAAASKSQPFVLA 65
           + LLIPGP  +   + +AL   +  HT P  V  F+  L  T+ +F +      + FV+A
Sbjct: 5   EMLLIPGPTPVVDEIYEALAQETYSHTDPRLVKRFKNSLDMTKRLFNT----DGEVFVVA 60

Query: 66  GSGTLGWDIFASNFILSKAPNKNVLVVSTGTFSDRFADCLRSYGAQVDVVRPLKIGESVP 125
           GSGTL  ++   N +   AP + +LV+S G F DRF    +++G QV+V++  + G+ V 
Sbjct: 61  GSGTLSMEMAIVNTV---APGEKILVISHGYFGDRFIPLAQAHGIQVEVLQS-QWGKHVE 116

Query: 126 LELITEKLSQNSYGAVTVTHVDTSTAVLSDLKAISQAIKQTSPETFFVVDAVCSIGC--- 182
           +  + EKL++  + AVTVTH DTST V+S+L+ +  A+K+  P   F++D VC+      
Sbjct: 117 ISAVEEKLAEGGFKAVTVTHADTSTGVMSNLEELVPAVKKYGP--LFILDGVCASAAIEE 174

Query: 183 ---EEFEFDEWGVDFALTASQKAIGAPAGLSISLCSSRFMDYALNDSKNGHVHGYFSSLR 239
              +E+   ++ +D  LT SQKAIG P GL+I     + +       K   V  Y+  + 
Sbjct: 175 NMQKEYGHPDYRIDLVLTGSQKAIGVPPGLAIVAFGPKALKAREAMDK---VAAYYMDIL 231

Query: 240 RWTPIMENYEAGKGAYFATPPVQLINSLDVALKEILEEGLHKRWDLHREMSDWFKDSLVN 299
           RW P M++     G Y+AT PV +I + +  ++ ++ EGL  R+  H  +    +  L  
Sbjct: 232 RWLPTMQD----PGKYYATHPVNMIYAYEKGMELVMAEGLEARYKRHAALGKAVRAGLA- 286

Query: 300 GLQLTSVSRYPSNMSAHGLTAVYVADPPDVIAF---LKSHGVVIAGGIHKDIGPKYIRIG 356
             Q    +  P  ++A  L+ +   +  +   F   L   G+VIAG +  ++  K  RIG
Sbjct: 287 --QYGMRALAPEEIAAPTLSCILYPEGVNDAEFRSKLAEKGMVIAGSL-ANLAGKAFRIG 343

Query: 357 HMG 359
           HMG
Sbjct: 344 HMG 346


Lambda     K      H
   0.319    0.134    0.397 

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: 356
Number of extensions: 19
Number of successful extensions: 7
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: 385
Length of database: 390
Length adjustment: 30
Effective length of query: 355
Effective length of database: 360
Effective search space:   127800
Effective search space used:   127800
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 10 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