GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potA in Sinorhizobium meliloti 1021

Align PotG aka B0855, component of Putrescine porter (characterized)
to candidate SMa1754 SMa1754 ABC transporter ATP-binding protein

Query= TCDB::P31134
         (377 letters)



>FitnessBrowser__Smeli:SMa1754
          Length = 359

 Score =  276 bits (707), Expect = 5e-79
 Identities = 151/361 (41%), Positives = 224/361 (62%), Gaps = 7/361 (1%)

Query: 15  ALTPLLEIRNLTKSYDGQHAVDDVSLTIYKGEIFALLGASGCGKSTLLRMLAGFEQPSAG 74
           ++   ++   +TK Y     V+++ L I +GE  +LLG SG GK+TLL MLAGFEQP++G
Sbjct: 4   SVAEFIQFDRITKFYGPLCVVENLVLGIGQGEFVSLLGPSGSGKTTLLMMLAGFEQPTSG 63

Query: 75  QIMLDGVDLSQVPPYLRPINMMFQSYALFPHMTVEQNIAFGLKQDKLPKAEIASRVNEML 134
            I+LDG  ++ VP + R + ++FQSYALFPHM+V +N+AF L+   L KAEIA  V   L
Sbjct: 64  NILLDGTAINDVPTHKRDMGVVFQSYALFPHMSVGENVAFPLQMRGLGKAEIAECVARAL 123

Query: 135 GLVHMQEFAKRKPHQLSGGQRQRVALARSLAKRPKLLLLDEPMGALDKKLRDRMQLEVVD 194
            +V +  FA R+P QLSGGQ+QRVAL+R+L   P+++L+DEP+GALDK+LR++MQ ++ D
Sbjct: 124 DMVQLSAFADRRPSQLSGGQQQRVALSRALVFEPRVVLMDEPLGALDKQLREQMQFDIRD 183

Query: 195 ILERVGVTCVMVTHDQEEAMTMAGRIAIMNRGKFVQIGEPEEIYEHPTTRYSAEFIGSVN 254
           +  R+G+T V VTHDQ EA+TM+ R+A+ NRGK  QIG P ++Y+ P TR+ AEFIG  N
Sbjct: 184 LHRRLGLTIVFVTHDQSEALTMSDRVAVFNRGKIEQIGTPRQVYDEPATRFVAEFIGETN 243

Query: 255 VFEGVLKERQEDGLVLDSPGLVHPLKVDADASVVDNVPVHVALRPEKIMLCEEPPANGCN 314
           + EGV++  Q    ++  P   H +      S+V    V +++RPE++ L  E   +  N
Sbjct: 244 LVEGVVETVQGQEAIVRLPSGAHIVSA-GSGSLVSGQSVFLSIRPERVDL-SETRGDARN 301

Query: 315 FAVGEVIHIAYLGDLSVYHVRLKSGQMISAQLQNAHRHRKGLPTWGDEVRLCWEVDSCVV 374
               EV    Y GD    H+R++        +    R  +  P  G +V   +  + C V
Sbjct: 302 CLETEVTDSVYQGD----HLRVQLQSAAHPLIAKLGRRSREFPP-GTKVYAAFSANDCRV 356

Query: 375 L 375
           +
Sbjct: 357 I 357


Lambda     K      H
   0.321    0.137    0.400 

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: 354
Number of extensions: 10
Number of successful extensions: 1
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: 377
Length of database: 359
Length adjustment: 30
Effective length of query: 347
Effective length of database: 329
Effective search space:   114163
Effective search space used:   114163
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 Sep 17 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