GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysY in Stenotrophomonas chelatiphaga DSM 21508

Align Putative [LysW]-L-2-aminoadipate/[LysW]-L-glutamate phosphate reductase; EC 1.2.1.103; EC 1.2.1.106 (uncharacterized)
to candidate WP_057687249.1 ABB28_RS15365 N-acetyl-gamma-glutamyl-phosphate reductase

Query= curated2:Q5UZ50
         (345 letters)



>NCBI__GCF_001431535.1:WP_057687249.1
          Length = 317

 Score =  152 bits (384), Expect = 1e-41
 Identities = 108/344 (31%), Positives = 169/344 (49%), Gaps = 44/344 (12%)

Query: 2   TYTASVVGGSGFTGGELLRLLDGHPEFELAQATSRSKENKTIGHSHPNLRHSDLRFSSPE 61
           T+T  +VG  G TG EL++L+  HP  +LA  +SR +  + +   HP +   ++++ + +
Sbjct: 5   TFTLGIVGARGHTGAELIKLVAAHPNLQLAFVSSRERAGQRLADHHPEIT-GEVQYENLD 63

Query: 62  D----LESVDVLFAATPHGVSMEQIDAFQEAAG--TVVDLSADFRLESEAQYDEWYDGHT 115
                 + VD +  A P+G++   + A + A     +VDLSAD+R E       WY    
Sbjct: 64  ADAVAAKGVDAVILALPNGLAAPFVAALESARPDTVIVDLSADYRFEGS-----WY---- 114

Query: 116 RPKLLEQSEYALPELNRDNLEGADLIASGGCNATATILGLLPLFEADILSGDEQIVVDVK 175
                    Y LPEL R    G   I++ GC ATA  L + PL   D+L+G  Q      
Sbjct: 115 ---------YGLPELTRTQYNGEKHISNPGCYATAMQLAIHPLL--DLLAGPPQCF---- 159

Query: 176 VGSSEGGAGGGEASS---HPER-SGVVRPYAPTGHRHEAEIQQFLGIDVSFTVHAVDMIR 231
                G +G G   S   +PE  +  + PYA T H HE E+   L + V F  H     R
Sbjct: 160 --GVSGYSGAGTTPSDKNNPELLADNLMPYALTNHVHEREVSAHLRVPVEFMPHVAPHFR 217

Query: 232 GASATCHVFPEQRVSKGDLWGAYRGEYEDEPFVELVAGGGGVYRYPEPKSVAGTNRAEVG 291
           G + T +++  Q  ++  +   +   Y  EP V++V     V R      +AG +  +VG
Sbjct: 218 GITMTVNLWLNQVQTREQIAARFADAYAAEPLVDVVDDAPWVSR------IAGRHGVQVG 271

Query: 292 -FELDPGNKRLVVFSAIDNMMKGSAGQAVHAANVALGIEETAGL 334
            F + PG KR+VV + +DN++KG+A QA+   N+ALGI+E   +
Sbjct: 272 GFTVAPGGKRVVVVATLDNLLKGAATQAMQNLNLALGIDELTSI 315


Lambda     K      H
   0.314    0.134    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: 313
Number of extensions: 23
Number of successful extensions: 5
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: 345
Length of database: 317
Length adjustment: 28
Effective length of query: 317
Effective length of database: 289
Effective search space:    91613
Effective search space used:    91613
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: 42 (21.9 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 2024.

Links

Downloads

Related tools

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