GapMind for Amino acid biosynthesis

 

Alignments for a candidate for glnA in Lacinutrix algicola AKS293

Align Glutamine synthetase; GS; Glutamate--ammonia ligase; Glutamine synthetase II; GSII; EC 6.3.1.2 (characterized)
to candidate WP_055435842.1 ASC41_RS06570 glutamine synthetase

Query= SwissProt::Q02154
         (326 letters)



>NCBI__GCF_001418085.1:WP_055435842.1
          Length = 338

 Score =  398 bits (1023), Expect = e-116
 Identities = 201/331 (60%), Positives = 239/331 (72%), Gaps = 8/331 (2%)

Query: 1   MTKFKLEYIWLDGYTPVPNLRGKTQIKEFDEFP-TLEQLPLWGFDGSSTMQAEG-SSDCV 58
           M K KLEYIWLDGY P  N+R KT+++E + F  T+E+L LW FDGSST QA G +SDC+
Sbjct: 1   MAKIKLEYIWLDGYYPTQNMRSKTKVEEHENFKGTVEELGLWSFDGSSTKQASGGASDCI 60

Query: 59  LKPVAIYPDPARTNGALVMCEVMMPDGHAHASNARATILDDE-DAWFGFEQEYFFYQNGR 117
           LKPVAIYPDP R NG LVM EVM  DG  H SNARATI DD+ D WFGFEQEYF      
Sbjct: 61  LKPVAIYPDPTRRNGYLVMTEVMNADGTPHISNARATIEDDDNDFWFGFEQEYFIMNTST 120

Query: 118 --PLGFPEQGYPAPQP-YYTGVGYSNVGDVAREIVEEHLDLCLAAGINHEGINAEVAKGQ 174
             PLGFP  GYPAPQ  YY  VG  +     R++VEEH DLC+ AG+N EGIN EVA GQ
Sbjct: 121 ELPLGFPRGGYPAPQGMYYCSVGGKHTH--GRDLVEEHADLCIDAGLNFEGINQEVASGQ 178

Query: 175 WEFQIFGKGSKKAADQIWMARYLLQRLTEKYGIDIEYHCKPLGDTDWNGSGMHCNFSTKY 234
           WE+Q+F KG+KKA D+IW++RYLL RLTE  G+ IEYH KPLG+TDWNGSGMH NFS   
Sbjct: 179 WEYQLFAKGAKKAGDEIWISRYLLDRLTEGKGMYIEYHPKPLGNTDWNGSGMHANFSNTI 238

Query: 235 LREVGGKEYFEALMASSDKNLMDHIAVYGPDNDKRLTGKHETAPWNKFSYGVADRGASIR 294
           LR  G KE +  +  +    + +HI VYG  N++RLTG HETA  N FS+GV+DRGASIR
Sbjct: 239 LRTCGSKEKYAEICEAFRPLVKEHIEVYGEHNEQRLTGDHETASINDFSWGVSDRGASIR 298

Query: 295 VPHSFIKNDYKGYLEDRRPNSQGDPYQIVRR 325
           +P   ++  YKG+LEDRRP+S GDPY+I  R
Sbjct: 299 IPIIAVEKGYKGWLEDRRPSSNGDPYKIAAR 329


Lambda     K      H
   0.319    0.138    0.438 

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: 492
Number of extensions: 20
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: 326
Length of database: 338
Length adjustment: 28
Effective length of query: 298
Effective length of database: 310
Effective search space:    92380
Effective search space used:    92380
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 26 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