GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysY in Trichodesmium erythraeum IMS101 Annotated Metagenome-Assembled Genome

Align [LysW]-L-2-aminoadipate/[LysW]-L-glutamate phosphate reductase; EC 1.2.1.103; EC 1.2.1.106 (uncharacterized)
to candidate 2629597979 Ga0074568_1143 N-acetyl-gamma-glutamyl-phosphate reductase

Query= curated2:Q976J5
         (349 letters)



>IMG__TrieryIMS101_FD:2629597979
          Length = 352

 Score =  246 bits (628), Expect = 6e-70
 Identities = 129/341 (37%), Positives = 195/341 (57%), Gaps = 3/341 (0%)

Query: 2   IRVAVIGGSGYTGGELLRILAVHPKIEVTYVTSREYAGKPITLVHPNLRGFYNMNFSQFS 61
           + + ++G SGY G +L+++L  HPK+EV Y+     AGKP + ++P+L    ++      
Sbjct: 7   VPIGIVGASGYGGVQLVKLLQNHPKVEVVYLGGDSSAGKPFSSIYPHLEHSVDLKIESIE 66

Query: 62  FDKLGDKADAVFLGLPHKVSLEYVPKILEMGIQVIDLSADFRLKDPTLYKIWYGYEHPYP 121
            DK+ +K+  VFL LP+ ++ +  P +LE G +V+DLSAD+R  +   Y+ WYG E    
Sbjct: 67  LDKIANKSQIVFLSLPNGLAWKMAPNLLEKGCKVLDLSADYRFSNLETYQSWYGGERTDQ 126

Query: 122 DLLKKAVYGLPELHYEELKNAKLIASPGCNATATILAGAPLVASSLLETYKLISDVKVGS 181
            +   AVYGLPEL+ + + NA+LI  PGC  TA++LA +PL    L+     I D K G+
Sbjct: 127 KIAATAVYGLPELYRDRIANAQLIGCPGCYVTASLLALSPLFKQGLIVPETAIIDAKSGT 186

Query: 182 SEGGAKPHEGSHHPERQNAIRPYEADGHRHAAEAEQELSLIAKRDVKVSLVPHAVSSVRG 241
           S GG K +      E  N++ PY    HRH  E EQ  S +A  DVKV   PH +  VRG
Sbjct: 187 SGGGRKANINMLLAEADNSVGPYGVASHRHTPEIEQICSNLAGYDVKVQFTPHLMPMVRG 246

Query: 242 ALASVHGWL-SSDISEMDMWKKSIEFYKGRKFIRIIRSNIHPYPDPKFVIGSNFADIGFA 300
            LA+V+G L    +   D+      FY+   +++++ S    YP  K+  G+N   +G  
Sbjct: 247 ILATVYGTLRDPGLVREDLLTIYNAFYRNCPWVKVLPSG--TYPQTKWASGTNLCYLGIE 304

Query: 301 IEKRMQRITMFSAIDNLMKGAAGQAVQAFNISRGFEEDEGL 341
           ++ R  R+ + SAIDNL+KG AGQ++Q  N+  G+EE  GL
Sbjct: 305 VDHRTDRVIIMSAIDNLIKGQAGQSIQCMNLMMGWEETLGL 345


Lambda     K      H
   0.319    0.137    0.405 

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: 376
Number of extensions: 13
Number of successful extensions: 2
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: 349
Length of database: 352
Length adjustment: 29
Effective length of query: 320
Effective length of database: 323
Effective search space:   103360
Effective search space used:   103360
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