GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gly1 in Nocardioides dokdonensis FR1436

Align L-threonine aldolase (EC 4.1.2.5) (characterized)
to candidate WP_068110556.1 I601_RS13330 GntG family PLP-dependent aldolase

Query= BRENDA::Q9X266
         (343 letters)



>NCBI__GCF_001653335.1:WP_068110556.1
          Length = 330

 Score =  283 bits (723), Expect = 6e-81
 Identities = 158/339 (46%), Positives = 216/339 (63%), Gaps = 10/339 (2%)

Query: 1   MIDLRSDTVTKPTEEMRKAMAQAEVGDDVYGEDPTINELERLAAETFGKEAALFVPSGTM 60
           MIDLRSDTVTKPTE MR AMA+AEVGDDVYGEDPT+ +LE   A   G EAALF+P+G+M
Sbjct: 1   MIDLRSDTVTKPTESMRAAMARAEVGDDVYGEDPTVLDLEEHVAGLLGHEAALFMPTGSM 60

Query: 61  GNQVSIMAHTQRGDEVILEADSHIFWYEVGAMAVLSGVMPHPVPGKNGAMDPDDVRKAIR 120
            N +++ A  + G EV+ EA +HI   E+GA A +SG+         G +D   V   + 
Sbjct: 61  ANVLAVRALVEPGQEVLCEASAHIARAELGAHAAISGLTMRTWIHPRGQLDLGAVASLVA 120

Query: 121 P-RNIHFPRTSLIAIENTHNRSGGRVVPLENIKEICTIAKEHGINVHIDGARIFNASIAS 179
           P     F RT+ +++ENTHN +GG V+P+ +++++  +A   GI VH+DGAR++NA +A+
Sbjct: 121 PDMGPFFVRTAAVSVENTHNFAGGTVLPMSDLRDLRELADGAGIAVHMDGARLWNAHVAT 180

Query: 180 GVPVKEYAGYADSVMFCLSKGLCAPVGSVVVGDRDFIERARKARKMLGGGMRQAGVLAAA 239
           G P+ EY   AD++  CLSKGL APVGS++VG  D +  AR  RK +GGGMRQ G+LAAA
Sbjct: 181 GTPLAEYGAVADTMAVCLSKGLGAPVGSLMVGSADAMVEARVRRKRMGGGMRQVGILAAA 240

Query: 240 GIIALTKMVDRLKEDHENARFLALKLKEIGYSVNPEDVKTNMVILRTDNLKVNAHGFIEA 299
           G  AL   +DRL +DHE+AR LA         V+P  V TN+V++  D    +A  F+  
Sbjct: 241 GRHALDHHLDRLADDHEHARLLA-----EACGVDPAGVDTNIVVVPHD----DAPDFVAR 291

Query: 300 LRNSGVLANAVSDTEIRLVTHKDVSRNDIEEALNIFEKL 338
             ++GV    V    +RLVTH  V+R D E+A  +   L
Sbjct: 292 AADAGVRVATVGPRTVRLVTHLGVTRADAEKAAAVLAGL 330


Lambda     K      H
   0.319    0.135    0.384 

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: 331
Number of extensions: 14
Number of successful extensions: 3
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: 343
Length of database: 330
Length adjustment: 28
Effective length of query: 315
Effective length of database: 302
Effective search space:    95130
Effective search space used:    95130
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: 49 (23.5 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