Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4IBP9
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009451 | RNA modification | 5 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0032259 | methylation | 2 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0043414 | macromolecule methylation | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0008168 | methyltransferase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.288 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.279 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.237 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.314 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.672 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.262 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.321 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.715 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.497 |
CLV_PCSK_PC1ET2_1 | 172 | 174 | PF00082 | 0.345 |
CLV_PCSK_PC1ET2_1 | 30 | 32 | PF00082 | 0.532 |
CLV_PCSK_PC1ET2_1 | 65 | 67 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 331 | 335 | PF00082 | 0.268 |
DEG_SPOP_SBC_1 | 209 | 213 | PF00917 | 0.435 |
DOC_ANK_TNKS_1 | 296 | 303 | PF00023 | 0.279 |
DOC_CKS1_1 | 201 | 206 | PF01111 | 0.279 |
DOC_CYCLIN_RxL_1 | 149 | 160 | PF00134 | 0.393 |
DOC_CYCLIN_yCln2_LP_2 | 175 | 178 | PF00134 | 0.195 |
DOC_MAPK_gen_1 | 354 | 360 | PF00069 | 0.431 |
DOC_MAPK_RevD_3 | 159 | 173 | PF00069 | 0.311 |
DOC_MAPK_RevD_3 | 248 | 264 | PF00069 | 0.288 |
DOC_MAPK_RevD_3 | 339 | 355 | PF00069 | 0.352 |
DOC_PP2B_LxvP_1 | 175 | 178 | PF13499 | 0.195 |
DOC_PP4_FxxP_1 | 201 | 204 | PF00568 | 0.377 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.388 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.335 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.252 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.378 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.598 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.326 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.373 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.231 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.613 |
LIG_14-3-3_CanoR_1 | 15 | 20 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 354 | 359 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 45 | 52 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 73 | 78 | PF00244 | 0.422 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.690 |
LIG_BRCT_BRCA1_1 | 244 | 248 | PF00533 | 0.263 |
LIG_BRCT_BRCA1_1 | 321 | 325 | PF00533 | 0.252 |
LIG_BRCT_BRCA1_1 | 356 | 360 | PF00533 | 0.487 |
LIG_Clathr_ClatBox_1 | 156 | 160 | PF01394 | 0.311 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.414 |
LIG_Integrin_RGD_1 | 299 | 301 | PF01839 | 0.328 |
LIG_LIR_Apic_2 | 198 | 204 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 126 | 132 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 242 | 250 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 242 | 246 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 322 | 327 | PF02991 | 0.252 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 42 | 47 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 89 | 93 | PF02991 | 0.252 |
LIG_MLH1_MIPbox_1 | 321 | 325 | PF16413 | 0.252 |
LIG_OCRL_FandH_1 | 79 | 91 | PF00620 | 0.363 |
LIG_PCNA_yPIPBox_3 | 316 | 325 | PF02747 | 0.252 |
LIG_Pex14_1 | 68 | 72 | PF04695 | 0.327 |
LIG_Pex14_2 | 360 | 364 | PF04695 | 0.471 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.267 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.252 |
LIG_SH3_1 | 33 | 39 | PF00018 | 0.559 |
LIG_SH3_2 | 10 | 15 | PF14604 | 0.547 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.249 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.575 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.569 |
LIG_SUMO_SIM_anti_2 | 242 | 248 | PF11976 | 0.395 |
LIG_SUMO_SIM_par_1 | 340 | 345 | PF11976 | 0.312 |
LIG_TRAF2_1 | 326 | 329 | PF00917 | 0.328 |
LIG_WRPW_2 | 44 | 47 | PF00400 | 0.480 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.409 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.342 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.446 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.345 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.259 |
MOD_Cter_Amidation | 27 | 30 | PF01082 | 0.552 |
MOD_DYRK1A_RPxSP_1 | 31 | 35 | PF00069 | 0.464 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.389 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.400 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.395 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.515 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.718 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.646 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.342 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.429 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.602 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.384 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.328 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.258 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.263 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.525 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.676 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.728 |
MOD_N-GLC_1 | 317 | 322 | PF02516 | 0.246 |
MOD_N-GLC_1 | 73 | 78 | PF02516 | 0.395 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.239 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.387 |
MOD_NEK2_2 | 197 | 202 | PF00069 | 0.195 |
MOD_PIKK_1 | 8 | 14 | PF00454 | 0.667 |
MOD_PK_1 | 354 | 360 | PF00069 | 0.501 |
MOD_PKA_1 | 354 | 360 | PF00069 | 0.452 |
MOD_PKA_1 | 380 | 386 | PF00069 | 0.598 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.527 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.696 |
MOD_PKB_1 | 368 | 376 | PF00069 | 0.387 |
MOD_Plk_1 | 159 | 165 | PF00069 | 0.280 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.232 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.393 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.316 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.259 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.326 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.373 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.231 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.610 |
TRG_DiLeu_BaEn_1 | 171 | 176 | PF01217 | 0.219 |
TRG_DiLeu_BaEn_1 | 242 | 247 | PF01217 | 0.363 |
TRG_DiLeu_BaEn_2 | 238 | 244 | PF01217 | 0.328 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.267 |
TRG_ENDOCYTIC_2 | 37 | 40 | PF00928 | 0.543 |
TRG_ER_diArg_1 | 262 | 264 | PF00400 | 0.288 |
TRG_ER_diArg_1 | 289 | 291 | PF00400 | 0.279 |
TRG_ER_diArg_1 | 296 | 299 | PF00400 | 0.369 |
TRG_ER_diArg_1 | 362 | 364 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 369 | 372 | PF00400 | 0.460 |
TRG_NLS_MonoExtC_3 | 28 | 33 | PF00514 | 0.555 |
TRG_NLS_MonoExtN_4 | 29 | 34 | PF00514 | 0.655 |
TRG_Pf-PMV_PEXEL_1 | 331 | 335 | PF00026 | 0.311 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4J3 | Leptomonas seymouri | 66% | 100% |
A0A0N1I1R8 | Leptomonas seymouri | 27% | 100% |
A0A0S4ISJ6 | Bodo saltans | 26% | 88% |
A0A0S4KFU5 | Bodo saltans | 35% | 100% |
A0A1X0NXB7 | Trypanosomatidae | 26% | 100% |
A0A1X0P5J2 | Trypanosomatidae | 44% | 100% |
A0A3Q8IDT0 | Leishmania donovani | 24% | 100% |
A0A3R7M2M3 | Trypanosoma rangeli | 45% | 100% |
A0A3S7X9Q3 | Leishmania donovani | 100% | 100% |
A0A422MZQ7 | Trypanosoma rangeli | 27% | 100% |
A4HBJ6 | Leishmania braziliensis | 27% | 100% |
A4HN30 | Leishmania braziliensis | 77% | 100% |
A4HZL8 | Leishmania infantum | 25% | 100% |
A8KBL7 | Danio rerio | 24% | 100% |
C9ZYX5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
D0A1J3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9AFI4 | Leishmania major | 93% | 100% |
E9AUW5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B6N9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q0P5B2 | Bos taurus | 25% | 100% |
Q4QCL7 | Leishmania major | 24% | 100% |
Q5RDV8 | Pongo abelii | 27% | 100% |
Q5ZHP8 | Gallus gallus | 23% | 100% |
Q6AXU8 | Rattus norvegicus | 28% | 100% |
Q6P1Q9 | Homo sapiens | 23% | 100% |
Q86BS6 | Drosophila melanogaster | 25% | 100% |
Q8BVH9 | Mus musculus | 27% | 100% |
Q8TCB7 | Homo sapiens | 27% | 100% |
Q96IZ6 | Homo sapiens | 23% | 100% |
V5BCV4 | Trypanosoma cruzi | 46% | 100% |
V5DGW7 | Trypanosoma cruzi | 27% | 100% |