GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gltX in Herbaspirillum seropedicae SmR1

Align glutamyl-tRNA(Glx) synthetase (EC 6.1.1.24) (characterized)
to candidate HSERO_RS17850 HSERO_RS17850 glutamyl-Q tRNA(Asp) ligase

Query= reanno::Caulo:CCNA_01982
         (470 letters)



>FitnessBrowser__HerbieS:HSERO_RS17850
          Length = 294

 Score =  127 bits (318), Expect = 6e-34
 Identities = 93/273 (34%), Positives = 138/273 (50%), Gaps = 15/273 (5%)

Query: 10  VTRFAPSPTGFLHIGGARTALFNWLYARHTGGKFLIRVEDTDRERSTEAAVAAIFEGLDW 69
           V RFAPSP+G LH G    AL ++L AR   G++L+R+ED D  R+ + A   I   L  
Sbjct: 7   VGRFAPSPSGPLHAGSLVAALASYLDARVHAGRWLLRIEDIDETRTVQGAAQDIIATLAA 66

Query: 70  LGLKSDDEVIFQHTRAPRHVEVVHELLAKGRAYRCWMSIEELEVAREKARAEGRAIRSPW 129
           L ++SD  V+ Q  R  R+ ++  + L    AY C  S +E+  +R    ++G A+    
Sbjct: 67  LDMRSDGPVLVQSQRKARY-QLARDRLG-ALAYPCGCSRKEIADSRVGTASDGAALYPGT 124

Query: 130 RDAPEGDLSAPHVIRFKGPLDGETLVNDLVK------GP-VTFKNIELDDLVLLRADGAP 182
                        +R + P  G+    +LV+      GP       E+ D VL RADG  
Sbjct: 125 CRHGLAPGKQARTLRLRVPDPGQA--GELVQFEDRWLGPQAQHLAAEVGDFVLQRADGFW 182

Query: 183 TYNLAVVVDDHDMGVTHVIRGDDHLNNAARQTLIYQAMDWAVPAFAHIPLIHGPDGAKLS 242
            Y LAVVVDD + GVT ++RG D L++ ARQ  +   + +  P + H+PL+    G K S
Sbjct: 183 AYQLAVVVDDAEQGVTDIVRGADLLDSTARQIYLQGLLGYPTPRYLHVPLLMNETGEKFS 242

Query: 243 KRHGAQAVGEFADLGYIPEGMRNYLARLGWGHG 275
           K++GAQA+    DL    + ++   A LG   G
Sbjct: 243 KQNGAQAL----DLNQPLQALQQAAAFLGLDTG 271



 Score = 23.5 bits (49), Expect = 0.010
 Identities = 13/28 (46%), Positives = 16/28 (57%)

Query: 440 GAQAPDLNKTMAALSRDEAIGRLDDALA 467
           GAQA DLN+ + AL +  A   LD   A
Sbjct: 246 GAQALDLNQPLQALQQAAAFLGLDTGAA 273


Lambda     K      H
   0.319    0.135    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: 349
Number of extensions: 14
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 470
Length of database: 294
Length adjustment: 30
Effective length of query: 440
Effective length of database: 264
Effective search space:   116160
Effective search space used:   116160
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