GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livM in Methylobacterium nodulans ORS 2060

Align High-affinity branched-chain amino acid transport system permease protein LivM; LIV-I protein M (characterized)
to candidate WP_015930502.1 MNOD_RS18710 branched-chain amino acid ABC transporter permease

Query= SwissProt::P22729
         (425 letters)



>NCBI__GCF_000022085.1:WP_015930502.1
          Length = 295

 Score =  144 bits (364), Expect = 3e-39
 Identities = 101/308 (32%), Positives = 161/308 (52%), Gaps = 37/308 (12%)

Query: 112 VDIATLTMIYIILGLGLNVVVGLSGLLVLGYGGFYAIGAYTFALLNHYYGLGFWTCLPIA 171
           + I  ++ IY++L LGLN+  GL+G+   G+ GF+ IGAYT ALL+       W    +A
Sbjct: 6   IAILIISGIYVLLALGLNLQYGLTGITNFGHVGFFCIGAYTAALLSQVSVP--WPFAFLA 63

Query: 172 GL-MAAAAGFLLGFPVLRLRGDYLAIVTLGFGEIVRILLLNNTEITGGPNGISQIPKPTL 230
           G  +AA   + LG   L+LR DY AIV+LGF E+VRI++ +   +T G  GI+ IPK  L
Sbjct: 64  GAALAALTAWPLGLISLKLRDDYFAIVSLGFSEVVRIVVTSEKWLTKGVQGITGIPK--L 121

Query: 231 FGLEFSRTAREGGWDTFSNFFGLKYDPSDRVIFLYLVALLLVVLSLFVINRLLRMPLGRA 290
           F                  F G     +  V+ L +   +L  LS    +R++R P GR 
Sbjct: 122 FA-----------------FLGTGITQAVAVLLLLVAVNVLAGLSK---SRIVRSPFGRM 161

Query: 291 WEALREDEIACRSLGLSPRRIKLTAFTISAAFAGFAGTLFAARQGFVSPESFTFAESAFV 350
            EA+R++E A ++LG  P + K+    + AA AG AG  +A   G++ PE F    + ++
Sbjct: 162 IEAIRDNEEAVKALGKDPSKFKIQVLMLGAALAGIAGGFYAHYIGYIVPEQFVPLITFYI 221

Query: 351 LAIVVLGGMGSQFAVILAAILLV-------VSRELMRDFNEYSML-----MLGGLMVLMM 398
              +++GG+G     ++  ++L+         R L+   +E  M      ++G  +VL  
Sbjct: 222 WMAIIIGGVGPISGALVGTLILMFFLEGSRFLRGLIPFVSEVEMASIRLGVIGLALVLFT 281

Query: 399 IWRPQGLL 406
           ++RPQGL+
Sbjct: 282 LYRPQGLM 289


Lambda     K      H
   0.330    0.145    0.436 

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: 253
Number of extensions: 9
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: 425
Length of database: 295
Length adjustment: 29
Effective length of query: 396
Effective length of database: 266
Effective search space:   105336
Effective search space used:   105336
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.8 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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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