Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_068105462.1 I601_RS01380 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_001653335.1:WP_068105462.1 Length = 506 Score = 313 bits (803), Expect = 7e-90 Identities = 190/486 (39%), Positives = 266/486 (54%), Gaps = 18/486 (3%) Query: 23 FINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVWSQLAPAK 82 +I+G + DA G T + P DG + V+ DA AV AR+ F++G W + Sbjct: 5 YIDGTWRDAADGATRDIHCPADGHHVVTVSEGGEQDAVAAVVAARSAFDNGPWPHTPAPE 64 Query: 83 RKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAI-HWTAEAIDKVYDE 141 R A L R AD L + +E+A LE+LD GK +S ID+ H+ + A + Sbjct: 65 RAALLHRLADRLEADKDEVARLESLDTGKRFVESQ-IDVDDIVSVFRHFASLAQGEAGRV 123 Query: 142 VAPTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSEKSPLTAI 201 V + V EP+GV I PWN+PLL WK+ P LA GN+ +LKPSE +P TAI Sbjct: 124 VDAGMPGVVSRVVHEPIGVCTLITPWNYPLLQTSWKVAPCLAAGNTFILKPSELTPSTAI 183 Query: 202 RIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMVYAGESNM 261 + +AG+P GV N++ G G VG L +VD + FTG +++MV A + Sbjct: 184 WLMGALSDAGLPDGVANLVLGAGDRVGPTLTEAPEVDLVSFTGGVVTGRRVMV-AAAPTV 242 Query: 262 KRIWLEAGGKSPNIVFADAPDLQAAAEAAASAIAFNQGEVCTAGSRLLVERSIKDKFLPM 321 K++ LE GGK+PN++FADA DL AA + A +A+ + G+VC+AG+RL+VE ++ D+ + Sbjct: 243 KKVALELGGKNPNVIFADA-DLDAAIDNALTAVFLDSGQVCSAGARLVVEDTVHDQVVDE 301 Query: 322 VVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGGKRTLEETG-- 379 +V + G P D G L+ + V +Y+ AG +GA L GG R E G Sbjct: 302 LVRRAGRIRLGGPFDDDAETGPLISAAHRDKVEAYVAAGIAEGATLRVGGGRP-EGAGYA 360 Query: 380 -----GTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAF-----DTAEE-AVAIANDTPYG 428 G Y PTI D + M QEE FGPVL+V F D EE AV+IANDT YG Sbjct: 361 AGLAEGFYYLPTILDDCSADMSCVQEESFGPVLTVERFTGEDADAREEAAVSIANDTVYG 420 Query: 429 LAAGIWTSDISKAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKYT 488 LA +WTSD +A + A +R G++W+N Y A +GG+KQSG GR+ + LE+Y Sbjct: 421 LAGAVWTSDAGRAERVASRLRHGTIWINDYHPYVAQAEWGGYKQSGTGRELGIAGLEEYR 480 Query: 489 ELKATW 494 E K W Sbjct: 481 ETKHIW 486 Lambda K H 0.316 0.132 0.390 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: 684 Number of extensions: 36 Number of successful extensions: 6 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: 497 Length of database: 506 Length adjustment: 34 Effective length of query: 463 Effective length of database: 472 Effective search space: 218536 Effective search space used: 218536 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.6 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.
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:
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