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:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HG25
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 245 | 249 | PF00656 | 0.575 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.358 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.769 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 376 | 378 | PF00675 | 0.552 |
CLV_PCSK_FUR_1 | 130 | 134 | PF00082 | 0.351 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 376 | 378 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.448 |
DEG_APCC_DBOX_1 | 334 | 342 | PF00400 | 0.476 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.634 |
DOC_CYCLIN_yCln2_LP_2 | 228 | 231 | PF00134 | 0.464 |
DOC_MAPK_MEF2A_6 | 202 | 209 | PF00069 | 0.631 |
DOC_PP2B_LxvP_1 | 228 | 231 | PF13499 | 0.635 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 383 | 387 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.678 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.692 |
LIG_14-3-3_CanoR_1 | 14 | 23 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 258 | 268 | PF00244 | 0.617 |
LIG_14-3-3_CanoR_1 | 316 | 323 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 339 | 345 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 365 | 370 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 405 | 410 | PF00244 | 0.600 |
LIG_BRCT_BRCA1_1 | 72 | 76 | PF00533 | 0.299 |
LIG_deltaCOP1_diTrp_1 | 434 | 438 | PF00928 | 0.613 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.613 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.333 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.399 |
LIG_FHA_2 | 126 | 132 | PF00498 | 0.411 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.662 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.519 |
LIG_LIR_Apic_2 | 434 | 439 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 353 | 363 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 364 | 375 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 410 | 421 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 237 | 241 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 410 | 416 | PF02991 | 0.592 |
LIG_NRBOX | 344 | 350 | PF00104 | 0.550 |
LIG_PDZ_Class_1 | 437 | 442 | PF00595 | 0.454 |
LIG_SH2_CRK | 98 | 102 | PF00017 | 0.290 |
LIG_SH2_PTP2 | 279 | 282 | PF00017 | 0.445 |
LIG_SH2_PTP2 | 413 | 416 | PF00017 | 0.592 |
LIG_SH2_SRC | 279 | 282 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 137 | 141 | PF00017 | 0.484 |
LIG_SH2_STAP1 | 38 | 42 | PF00017 | 0.454 |
LIG_SH2_STAP1 | 409 | 413 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.656 |
LIG_SH3_2 | 231 | 236 | PF14604 | 0.460 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.488 |
LIG_SUMO_SIM_anti_2 | 172 | 179 | PF11976 | 0.522 |
LIG_SUMO_SIM_anti_2 | 54 | 59 | PF11976 | 0.573 |
LIG_SUMO_SIM_par_1 | 203 | 212 | PF11976 | 0.551 |
LIG_TRAF2_1 | 170 | 173 | PF00917 | 0.664 |
LIG_TRAF2_1 | 249 | 252 | PF00917 | 0.461 |
LIG_TRAF2_1 | 282 | 285 | PF00917 | 0.534 |
LIG_UBA3_1 | 206 | 210 | PF00899 | 0.489 |
LIG_UBA3_1 | 66 | 75 | PF00899 | 0.453 |
MOD_CDK_SPxxK_3 | 229 | 236 | PF00069 | 0.461 |
MOD_CDK_SPxxK_3 | 388 | 395 | PF00069 | 0.462 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.585 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.519 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.477 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.627 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.474 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.468 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.565 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.588 |
MOD_GlcNHglycan | 211 | 216 | PF01048 | 0.612 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.761 |
MOD_GlcNHglycan | 251 | 255 | PF01048 | 0.678 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.456 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.570 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.578 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.586 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.527 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.420 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.654 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.684 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.519 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.406 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.484 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.357 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.620 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.536 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.436 |
MOD_N-GLC_1 | 224 | 229 | PF02516 | 0.489 |
MOD_N-GLC_1 | 70 | 75 | PF02516 | 0.303 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.642 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.550 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.391 |
MOD_NEK2_2 | 205 | 210 | PF00069 | 0.485 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.493 |
MOD_PIKK_1 | 159 | 165 | PF00454 | 0.473 |
MOD_PIKK_1 | 268 | 274 | PF00454 | 0.570 |
MOD_PIKK_1 | 315 | 321 | PF00454 | 0.426 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.569 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.517 |
MOD_PKB_1 | 12 | 20 | PF00069 | 0.324 |
MOD_PKB_1 | 395 | 403 | PF00069 | 0.474 |
MOD_Plk_1 | 149 | 155 | PF00069 | 0.611 |
MOD_Plk_1 | 18 | 24 | PF00069 | 0.532 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.484 |
MOD_Plk_2-3 | 125 | 131 | PF00069 | 0.352 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.484 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.532 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.710 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.535 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.531 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.658 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.462 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.489 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.700 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.588 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.696 |
TRG_DiLeu_BaEn_1 | 284 | 289 | PF01217 | 0.517 |
TRG_DiLeu_BaEn_1 | 52 | 57 | PF01217 | 0.585 |
TRG_DiLeu_BaEn_4 | 284 | 290 | PF01217 | 0.523 |
TRG_DiLeu_BaLyEn_6 | 202 | 207 | PF01217 | 0.484 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 413 | 416 | PF00928 | 0.592 |
TRG_ENDOCYTIC_2 | 98 | 101 | PF00928 | 0.378 |
TRG_ER_diArg_1 | 11 | 14 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 115 | 117 | PF00400 | 0.332 |
TRG_ER_diArg_1 | 192 | 195 | PF00400 | 0.724 |
TRG_ER_diArg_1 | 257 | 259 | PF00400 | 0.619 |
TRG_ER_diArg_1 | 376 | 378 | PF00400 | 0.495 |
TRG_NES_CRM1_1 | 49 | 61 | PF08389 | 0.370 |
TRG_Pf-PMV_PEXEL_1 | 121 | 125 | PF00026 | 0.521 |
TRG_Pf-PMV_PEXEL_1 | 146 | 150 | PF00026 | 0.471 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IB83 | Leptomonas seymouri | 45% | 100% |
A0A1X0NF90 | Trypanosomatidae | 30% | 100% |
A0A3R7KL96 | Trypanosoma rangeli | 30% | 100% |
A0A3S7X122 | Leishmania donovani | 73% | 99% |
A4I346 | Leishmania infantum | 73% | 99% |
C9ZJL9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9ACW5 | Leishmania major | 72% | 100% |
E9AZF4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 99% |
V5BB13 | Trypanosoma cruzi | 29% | 100% |