Although predicted to have a multi-helical architecture, the protein is not hydrophobic enough for a membrane protein.. Unique to kinetoplastids, fast-evolving and duplicated multiple times.
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 15 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 17 |
NetGPI | no | yes: 0, no: 17 |
Related structures:
AlphaFold database: A4HJ73
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 134 | 138 | PF00656 | 0.787 |
CLV_C14_Caspase3-7 | 140 | 144 | PF00656 | 0.694 |
CLV_C14_Caspase3-7 | 75 | 79 | PF00656 | 0.704 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 458 | 460 | PF00675 | 0.485 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.525 |
CLV_PCSK_PC1ET2_1 | 239 | 241 | PF00082 | 0.444 |
CLV_PCSK_PC1ET2_1 | 487 | 489 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 331 | 335 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 459 | 463 | PF00082 | 0.449 |
CLV_Separin_Metazoa | 456 | 460 | PF03568 | 0.448 |
DEG_APCC_DBOX_1 | 203 | 211 | PF00400 | 0.322 |
DEG_APCC_DBOX_1 | 29 | 37 | PF00400 | 0.361 |
DEG_SCF_FBW7_1 | 395 | 401 | PF00400 | 0.466 |
DOC_CKS1_1 | 395 | 400 | PF01111 | 0.472 |
DOC_CYCLIN_RxL_1 | 238 | 248 | PF00134 | 0.458 |
DOC_MAPK_gen_1 | 239 | 245 | PF00069 | 0.404 |
DOC_MAPK_MEF2A_6 | 156 | 164 | PF00069 | 0.671 |
DOC_MAPK_MEF2A_6 | 450 | 457 | PF00069 | 0.456 |
DOC_PP4_FxxP_1 | 471 | 474 | PF00568 | 0.524 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.716 |
DOC_USP7_MATH_2 | 341 | 347 | PF00917 | 0.739 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.797 |
DOC_WW_Pin1_4 | 473 | 478 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.585 |
LIG_14-3-3_CanoR_1 | 272 | 277 | PF00244 | 0.678 |
LIG_14-3-3_CanoR_1 | 30 | 38 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 376 | 382 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 413 | 417 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 434 | 438 | PF00244 | 0.647 |
LIG_AP2alpha_1 | 50 | 54 | PF02296 | 0.641 |
LIG_APCC_ABBAyCdc20_2 | 450 | 456 | PF00400 | 0.462 |
LIG_BIR_III_2 | 148 | 152 | PF00653 | 0.539 |
LIG_BRCT_BRCA1_1 | 274 | 278 | PF00533 | 0.679 |
LIG_CSL_BTD_1 | 395 | 398 | PF09270 | 0.755 |
LIG_eIF4E_1 | 290 | 296 | PF01652 | 0.398 |
LIG_EVH1_2 | 100 | 104 | PF00568 | 0.562 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.554 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.583 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.684 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.667 |
LIG_FHA_2 | 30 | 36 | PF00498 | 0.626 |
LIG_Integrin_RGD_1 | 76 | 78 | PF01839 | 0.592 |
LIG_LIR_Apic_2 | 470 | 474 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 167 | 177 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 184 | 193 | PF02991 | 0.600 |
LIG_LIR_Gen_1 | 247 | 257 | PF02991 | 0.614 |
LIG_LIR_Nem_3 | 159 | 164 | PF02991 | 0.638 |
LIG_LIR_Nem_3 | 17 | 23 | PF02991 | 0.653 |
LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 184 | 188 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 247 | 253 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 275 | 280 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 305 | 309 | PF02991 | 0.608 |
LIG_MLH1_MIPbox_1 | 274 | 278 | PF16413 | 0.405 |
LIG_Pex14_2 | 461 | 465 | PF04695 | 0.446 |
LIG_Pex14_2 | 50 | 54 | PF04695 | 0.641 |
LIG_SH2_CRK | 175 | 179 | PF00017 | 0.593 |
LIG_SH2_CRK | 20 | 24 | PF00017 | 0.650 |
LIG_SH2_CRK | 298 | 302 | PF00017 | 0.492 |
LIG_SH2_CRK | 306 | 310 | PF00017 | 0.433 |
LIG_SH2_CRK | 319 | 323 | PF00017 | 0.431 |
LIG_SH2_GRB2like | 319 | 322 | PF00017 | 0.428 |
LIG_SH2_SRC | 319 | 322 | PF00017 | 0.428 |
LIG_SH2_STAP1 | 319 | 323 | PF00017 | 0.431 |
LIG_SH2_STAT3 | 37 | 40 | PF00017 | 0.628 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.620 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.601 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.731 |
LIG_SH2_STAT5 | 37 | 40 | PF00017 | 0.628 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.824 |
LIG_SH3_2 | 474 | 479 | PF14604 | 0.525 |
LIG_SH3_3 | 350 | 356 | PF00018 | 0.495 |
LIG_SH3_3 | 392 | 398 | PF00018 | 0.772 |
LIG_SH3_3 | 471 | 477 | PF00018 | 0.520 |
LIG_SUMO_SIM_par_1 | 377 | 384 | PF11976 | 0.509 |
LIG_SUMO_SIM_par_1 | 405 | 411 | PF11976 | 0.438 |
LIG_TRAF2_1 | 415 | 418 | PF00917 | 0.584 |
LIG_TYR_ITIM | 18 | 23 | PF00017 | 0.644 |
LIG_TYR_ITIM | 296 | 301 | PF00017 | 0.422 |
LIG_UBA3_1 | 216 | 224 | PF00899 | 0.599 |
MOD_CDC14_SPxK_1 | 476 | 479 | PF00782 | 0.527 |
MOD_CDC14_SPxK_1 | 73 | 76 | PF00782 | 0.588 |
MOD_CDK_SPxK_1 | 473 | 479 | PF00069 | 0.525 |
MOD_CDK_SPxK_1 | 70 | 76 | PF00069 | 0.587 |
MOD_CDK_SPxxK_3 | 427 | 434 | PF00069 | 0.797 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.572 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.656 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.589 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.521 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.623 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.597 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.565 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.778 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.375 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.515 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.793 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.560 |
MOD_GlcNHglycan | 62 | 66 | PF01048 | 0.632 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.587 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.449 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.585 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.650 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.806 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.745 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.499 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.562 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.775 |
MOD_N-GLC_1 | 444 | 449 | PF02516 | 0.519 |
MOD_N-GLC_2 | 297 | 299 | PF02516 | 0.530 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.583 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.618 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.629 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.629 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.728 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.795 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.414 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.643 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.814 |
MOD_PIKK_1 | 210 | 216 | PF00454 | 0.581 |
MOD_PIKK_1 | 396 | 402 | PF00454 | 0.610 |
MOD_PK_1 | 4 | 10 | PF00069 | 0.836 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.623 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.663 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.648 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.608 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.681 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.309 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.316 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.751 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.797 |
MOD_ProDKin_1 | 473 | 479 | PF00069 | 0.525 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.587 |
TRG_DiLeu_BaLyEn_6 | 173 | 178 | PF01217 | 0.596 |
TRG_DiLeu_BaLyEn_6 | 402 | 407 | PF01217 | 0.703 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.568 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.647 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.279 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.561 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.609 |
TRG_ENDOCYTIC_2 | 298 | 301 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 306 | 309 | PF00928 | 0.394 |
TRG_ENDOCYTIC_2 | 319 | 322 | PF00928 | 0.428 |
TRG_Pf-PMV_PEXEL_1 | 176 | 180 | PF00026 | 0.601 |
TRG_Pf-PMV_PEXEL_1 | 355 | 360 | PF00026 | 0.515 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IFG5 | Leishmania donovani | 64% | 79% |
A0A3Q8ISI8 | Leishmania donovani | 65% | 79% |
A0A3S7X4A3 | Leishmania donovani | 64% | 79% |
A4HJ70 | Leishmania braziliensis | 88% | 100% |
A4HJ71 | Leishmania braziliensis | 94% | 100% |
A4I6I2 | Leishmania infantum | 64% | 75% |
A4I6L8 | Leishmania infantum | 64% | 79% |
E8NHD1 | Leishmania infantum | 65% | 83% |
E8NHD2 | Leishmania infantum | 69% | 100% |
E8NHE7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 65% | 79% |
E8NHE8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 79% |
E9B1P3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 79% |
Q4Q6G7 | Leishmania major | 66% | 100% |
Q4Q6G8 | Leishmania major | 65% | 100% |
Q4Q6H0 | Leishmania major | 66% | 100% |
Q9BHE5 | Leishmania major | 66% | 100% |