GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysY in Thiomicrospira microaerophila ASL8-2

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_044411826.1 NA59_RS10005 N-acetyl-gamma-glutamyl-phosphate reductase

Query= curated2:A0RWW0
         (348 letters)



>NCBI__GCF_000934765.1:WP_044411826.1
          Length = 348

 Score =  261 bits (666), Expect = 2e-74
 Identities = 143/350 (40%), Positives = 205/350 (58%), Gaps = 8/350 (2%)

Query: 1   MKVGVVGASGYVGGETLRLLVNHPDVEIAAVTSRQHVGEYLHRVQPSLRGFTDLTFSELD 60
           +KVG+VG +GY G E LRLL NHP  E+  +TSR   G  + ++ P+LRG  DL FSE D
Sbjct: 4   VKVGIVGGTGYTGVELLRLLANHPQAEVVVITSRSEAGMSVAQMFPNLRGHFDLCFSEPD 63

Query: 61  YDRLSDSCDLVFTAVPHGTATDIVRALYDRDIKVIDLSADYRLHDPADYTKWYGWEHPHP 120
             +L   CDLVF A PHG A  +   L +  ++VIDL+AD+RL D A + +WY   H  P
Sbjct: 64  MAQLK-RCDLVFFATPHGVAMSLTPELIEAGVRVIDLAADFRLTDMAVFEQWYDMPHSCP 122

Query: 121 DYLSKSVFGIPELHREEIRSAKLVSCPGCMAVTSILALAPPVREGLVDTEHIVVDSKIGS 180
           + +   V+G+PE++R++I++AK+++ PGC      LA  P ++ G++DT H++ D K G 
Sbjct: 123 EIMKDVVYGLPEVNRDKIKTAKVIANPGCYPTAIQLAFQPLLKAGIIDTRHLIADGKSGV 182

Query: 181 SGAGAGAGTA--HAMRAGVIRPYKPAKHRHTGEIEQELSGIA-GKKIRVSMSPHAVDVVR 237
           SGAG GA  A   A  +   R Y    HRH  EI + LS +A G K+ ++  PH V ++R
Sbjct: 183 SGAGRGAKVASLSAETSESFRAYGIDGHRHQPEISEGLSVMAGGGKVNLTFVPHLVPMIR 242

Query: 238 GILCTNHVFLTREASEKDLWKMYRQAYGEERFVRLIRDKKGLYKFPDPKFLVGSNFCDIG 297
           GI  T +  LT + S+  L  ++   Y +E+FV    D       PD + + GSN C + 
Sbjct: 243 GIEATIYAKLTADWSQSQLQDLFETQYADEKFV----DVMPAGSQPDTRMVKGSNMCRMA 298

Query: 298 FDLDEDNNRLVAISASDNLMKGAAGSAIQNMNIMAGLDEMSGLRYTPLTP 347
                  + +V  S  DNL+KGA+G A+QNMN+M GLDE  GL+   L P
Sbjct: 299 VYRPVGGDVVVVTSVIDNLVKGASGQAVQNMNLMFGLDEDCGLKQVALLP 348


Lambda     K      H
   0.320    0.137    0.412 

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: 287
Number of extensions: 14
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: 348
Length of database: 348
Length adjustment: 29
Effective length of query: 319
Effective length of database: 319
Effective search space:   101761
Effective search space used:   101761
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 (21.8 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 10 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