GapMind for Amino acid biosynthesis

 

Alignments for a candidate for glnA in Sinorhizobium meliloti 1021

Align Glutamine synthetase; GS; Glutamate--ammonia ligase; Glutamine synthetase II; GSII; EC 6.3.1.2 (characterized)
to candidate SM_b20745 SM_b20745 glutatmine synthetase II protein

Query= SwissProt::Q02154
         (326 letters)



>FitnessBrowser__Smeli:SM_b20745
          Length = 344

 Score =  609 bits (1571), Expect = e-179
 Identities = 284/325 (87%), Positives = 303/325 (93%), Gaps = 3/325 (0%)

Query: 1   MTKFKLEYIWLDGYTPVPNLRGKTQIKEFDEFPTLEQLPLWGFDGSSTMQAEG-SSDCVL 59
           MTK+KLEYIWLDGYTPVPNLRGKTQIKEFD FPTLEQLPLWGFDGSST QAEG SSDCVL
Sbjct: 1   MTKYKLEYIWLDGYTPVPNLRGKTQIKEFDAFPTLEQLPLWGFDGSSTQQAEGRSSDCVL 60

Query: 60  KPVAIYPDPARTNGALVMCEVMMPDGHA-HASNARATILDDEDAWFGFEQEYFFYQNGRP 118
           KPVA+YPDP RTNGALVMCEVMMPDG   H SN RAT+LDDE AWFGFEQEYFFY+NGRP
Sbjct: 61  KPVAVYPDPVRTNGALVMCEVMMPDGKTPHPSNTRATVLDDESAWFGFEQEYFFYKNGRP 120

Query: 119 LGFPEQGYPAPQ-PYYTGVGYSNVGDVAREIVEEHLDLCLAAGINHEGINAEVAKGQWEF 177
           LGFPEQGYPAPQ PYYTGVGY NVGD+AR+IVEEHLD+CLAAGINHEGINAEVAKGQWEF
Sbjct: 121 LGFPEQGYPAPQGPYYTGVGYKNVGDIARQIVEEHLDICLAAGINHEGINAEVAKGQWEF 180

Query: 178 QIFGKGSKKAADQIWMARYLLQRLTEKYGIDIEYHCKPLGDTDWNGSGMHCNFSTKYLRE 237
           Q+FGKGSKKAAD++W+ARYLL RLTEKYGID+E+HCKPLGDTDWNGSGMH NFST YLRE
Sbjct: 181 QVFGKGSKKAADEVWLARYLLLRLTEKYGIDVEFHCKPLGDTDWNGSGMHANFSTAYLRE 240

Query: 238 VGGKEYFEALMASSDKNLMDHIAVYGPDNDKRLTGKHETAPWNKFSYGVADRGASIRVPH 297
           VGGK+YFEALMA+ +KNL DHI VYGPDN  RLTGKHETAPW+KFSYGVADRGASIRVPH
Sbjct: 241 VGGKDYFEALMAAFEKNLHDHINVYGPDNHLRLTGKHETAPWDKFSYGVADRGASIRVPH 300

Query: 298 SFIKNDYKGYLEDRRPNSQGDPYQI 322
           SF+ N Y+GYLEDRRPNSQGDPYQI
Sbjct: 301 SFVNNGYRGYLEDRRPNSQGDPYQI 325


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: 569
Number of extensions: 12
Number of successful extensions: 4
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: 344
Length adjustment: 28
Effective length of query: 298
Effective length of database: 316
Effective search space:    94168
Effective search space used:    94168
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 Apr 09 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