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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4HN02
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006364 | rRNA processing | 8 | 11 |
GO:0006396 | RNA processing | 6 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0016072 | rRNA metabolic process | 7 | 11 |
GO:0032259 | methylation | 2 | 11 |
GO:0034470 | ncRNA processing | 7 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0034660 | ncRNA metabolic process | 6 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0008168 | methyltransferase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.263 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.263 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 414 | 416 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.403 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.711 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.609 |
CLV_PCSK_FUR_1 | 428 | 432 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.263 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.244 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 414 | 416 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.626 |
CLV_PCSK_PC1ET2_1 | 226 | 228 | PF00082 | 0.387 |
CLV_PCSK_PC1ET2_1 | 363 | 365 | PF00082 | 0.483 |
CLV_PCSK_PC1ET2_1 | 420 | 422 | PF00082 | 0.544 |
CLV_PCSK_PC1ET2_1 | 432 | 434 | PF00082 | 0.518 |
CLV_PCSK_PC7_1 | 421 | 427 | PF00082 | 0.574 |
CLV_PCSK_PC7_1 | 428 | 434 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.521 |
CLV_Separin_Metazoa | 111 | 115 | PF03568 | 0.396 |
CLV_Separin_Metazoa | 281 | 285 | PF03568 | 0.462 |
DEG_APCC_DBOX_1 | 153 | 161 | PF00400 | 0.562 |
DEG_APCC_DBOX_1 | 420 | 428 | PF00400 | 0.663 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.688 |
DEG_SPOP_SBC_1 | 39 | 43 | PF00917 | 0.712 |
DEG_SPOP_SBC_1 | 398 | 402 | PF00917 | 0.789 |
DOC_CKS1_1 | 47 | 52 | PF01111 | 0.475 |
DOC_CYCLIN_RxL_1 | 124 | 132 | PF00134 | 0.482 |
DOC_MAPK_gen_1 | 284 | 290 | PF00069 | 0.494 |
DOC_MAPK_gen_1 | 337 | 345 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 337 | 345 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 376 | 383 | PF00069 | 0.457 |
DOC_MAPK_NFAT4_5 | 338 | 346 | PF00069 | 0.396 |
DOC_PP1_RVXF_1 | 320 | 327 | PF00149 | 0.532 |
DOC_PP4_FxxP_1 | 9 | 12 | PF00568 | 0.455 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.402 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.775 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 397 | 401 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.622 |
DOC_USP7_UBL2_3 | 359 | 363 | PF12436 | 0.556 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.588 |
LIG_14-3-3_CanoR_1 | 147 | 157 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 301 | 311 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 52 | 61 | PF00244 | 0.508 |
LIG_14-3-3_CterR_2 | 460 | 462 | PF00244 | 0.508 |
LIG_BRCT_BRCA1_1 | 247 | 251 | PF00533 | 0.482 |
LIG_BRCT_BRCA1_1 | 61 | 65 | PF00533 | 0.644 |
LIG_EH1_1 | 368 | 376 | PF00400 | 0.388 |
LIG_EVH1_2 | 379 | 383 | PF00568 | 0.474 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.482 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.482 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.534 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.476 |
LIG_FHA_2 | 241 | 247 | PF00498 | 0.597 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.645 |
LIG_FHA_2 | 407 | 413 | PF00498 | 0.586 |
LIG_FHA_2 | 71 | 77 | PF00498 | 0.543 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.516 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 274 | 278 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.628 |
LIG_MAD2 | 264 | 272 | PF02301 | 0.584 |
LIG_MLH1_MIPbox_1 | 247 | 251 | PF16413 | 0.482 |
LIG_NRBOX | 156 | 162 | PF00104 | 0.482 |
LIG_Pex14_2 | 275 | 279 | PF04695 | 0.562 |
LIG_Pex14_2 | 61 | 65 | PF04695 | 0.694 |
LIG_SH2_CRK | 67 | 71 | PF00017 | 0.614 |
LIG_SH2_STAT3 | 14 | 17 | PF00017 | 0.466 |
LIG_SH2_STAT3 | 327 | 330 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.542 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.562 |
LIG_SH3_3 | 378 | 384 | PF00018 | 0.643 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.473 |
LIG_SUMO_SIM_anti_2 | 129 | 135 | PF11976 | 0.482 |
LIG_SUMO_SIM_anti_2 | 41 | 49 | PF11976 | 0.649 |
LIG_TRAF2_1 | 410 | 413 | PF00917 | 0.700 |
LIG_TRAF2_1 | 442 | 445 | PF00917 | 0.590 |
MOD_CDK_SPxK_1 | 46 | 52 | PF00069 | 0.518 |
MOD_CDK_SPxxK_3 | 46 | 53 | PF00069 | 0.475 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.369 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.345 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.620 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.447 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.490 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.745 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.447 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.335 |
MOD_CK2_1 | 406 | 412 | PF00069 | 0.724 |
MOD_CK2_1 | 439 | 445 | PF00069 | 0.600 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.335 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.365 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.348 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.279 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.361 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.221 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.680 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.749 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.753 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.698 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.793 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.419 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.605 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.447 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.404 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.316 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.403 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.604 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.780 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.662 |
MOD_N-GLC_1 | 148 | 153 | PF02516 | 0.335 |
MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.436 |
MOD_N-GLC_1 | 311 | 316 | PF02516 | 0.335 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.331 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.650 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.319 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.354 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.533 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.616 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.585 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.530 |
MOD_PIKK_1 | 24 | 30 | PF00454 | 0.678 |
MOD_PKA_1 | 52 | 58 | PF00069 | 0.602 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.378 |
MOD_PKA_2 | 367 | 373 | PF00069 | 0.571 |
MOD_PKA_2 | 385 | 391 | PF00069 | 0.720 |
MOD_PKA_2 | 52 | 58 | PF00069 | 0.659 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.605 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.335 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.215 |
MOD_Plk_1 | 311 | 317 | PF00069 | 0.335 |
MOD_Plk_1 | 456 | 462 | PF00069 | 0.725 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.335 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.335 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.463 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.335 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.420 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.598 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.676 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.585 |
MOD_SUMO_for_1 | 410 | 413 | PF00179 | 0.656 |
TRG_DiLeu_BaEn_1 | 331 | 336 | PF01217 | 0.482 |
TRG_DiLeu_BaLyEn_6 | 138 | 143 | PF01217 | 0.335 |
TRG_DiLeu_BaLyEn_6 | 432 | 437 | PF01217 | 0.566 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.620 |
TRG_ER_diArg_1 | 262 | 265 | PF00400 | 0.319 |
TRG_ER_diArg_1 | 283 | 285 | PF00400 | 0.308 |
TRG_ER_diArg_1 | 298 | 301 | PF00400 | 0.308 |
TRG_ER_diArg_1 | 364 | 366 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 414 | 417 | PF00400 | 0.589 |
TRG_ER_diArg_1 | 424 | 426 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 427 | 430 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 51 | 53 | PF00400 | 0.605 |
TRG_NLS_Bipartite_1 | 52 | 72 | PF00514 | 0.557 |
TRG_NLS_MonoCore_2 | 362 | 367 | PF00514 | 0.624 |
TRG_NLS_MonoExtC_3 | 416 | 421 | PF00514 | 0.655 |
TRG_NLS_MonoExtN_4 | 414 | 421 | PF00514 | 0.622 |
TRG_Pf-PMV_PEXEL_1 | 425 | 429 | PF00026 | 0.654 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4G3 | Leptomonas seymouri | 66% | 100% |
A0A1X0P5K8 | Trypanosomatidae | 54% | 100% |
A0A3R7N6Y9 | Trypanosoma rangeli | 55% | 100% |
A0A3S7X9K0 | Leishmania donovani | 84% | 100% |
A4IBM5 | Leishmania infantum | 84% | 100% |
C9ZZ09 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 100% |
E9AFF9 | Leishmania major | 84% | 100% |
E9B6L4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
V5BY28 | Trypanosoma cruzi | 64% | 100% |