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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4I0M1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.561 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.462 |
DEG_SPOP_SBC_1 | 333 | 337 | PF00917 | 0.621 |
DOC_ANK_TNKS_1 | 18 | 25 | PF00023 | 0.564 |
DOC_CDC14_PxL_1 | 413 | 421 | PF14671 | 0.538 |
DOC_CKS1_1 | 71 | 76 | PF01111 | 0.503 |
DOC_MAPK_DCC_7 | 404 | 413 | PF00069 | 0.623 |
DOC_MAPK_gen_1 | 10 | 16 | PF00069 | 0.473 |
DOC_MAPK_gen_1 | 219 | 228 | PF00069 | 0.508 |
DOC_MAPK_MEF2A_6 | 219 | 228 | PF00069 | 0.508 |
DOC_MAPK_MEF2A_6 | 404 | 413 | PF00069 | 0.623 |
DOC_MAPK_NFAT4_5 | 223 | 231 | PF00069 | 0.536 |
DOC_PP4_FxxP_1 | 213 | 216 | PF00568 | 0.573 |
DOC_PP4_FxxP_1 | 71 | 74 | PF00568 | 0.493 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 447 | 451 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.628 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.499 |
LIG_14-3-3_CanoR_1 | 118 | 123 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 194 | 202 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 260 | 268 | PF00244 | 0.716 |
LIG_14-3-3_CanoR_1 | 286 | 293 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 31 | 35 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 51 | 57 | PF00244 | 0.489 |
LIG_AP2alpha_1 | 360 | 364 | PF02296 | 0.391 |
LIG_AP2alpha_2 | 299 | 301 | PF02296 | 0.574 |
LIG_APCC_ABBA_1 | 12 | 17 | PF00400 | 0.420 |
LIG_APCC_ABBAyCdc20_2 | 11 | 17 | PF00400 | 0.470 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.655 |
LIG_BIR_III_2 | 162 | 166 | PF00653 | 0.503 |
LIG_BRCT_BRCA1_1 | 447 | 451 | PF00533 | 0.520 |
LIG_CtBP_PxDLS_1 | 408 | 412 | PF00389 | 0.658 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.439 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.491 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.514 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.669 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.488 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.513 |
LIG_FHA_2 | 180 | 186 | PF00498 | 0.514 |
LIG_FHA_2 | 370 | 376 | PF00498 | 0.622 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.620 |
LIG_LIR_Apic_2 | 211 | 216 | PF02991 | 0.565 |
LIG_LIR_Apic_2 | 69 | 74 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 175 | 183 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 299 | 309 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 175 | 179 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 211 | 215 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 299 | 304 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 43 | 49 | PF02991 | 0.546 |
LIG_NRBOX | 452 | 458 | PF00104 | 0.539 |
LIG_PCNA_PIPBox_1 | 206 | 215 | PF02747 | 0.481 |
LIG_Pex14_2 | 360 | 364 | PF04695 | 0.445 |
LIG_Pex14_2 | 391 | 395 | PF04695 | 0.467 |
LIG_Pex14_2 | 71 | 75 | PF04695 | 0.470 |
LIG_REV1ctd_RIR_1 | 13 | 23 | PF16727 | 0.467 |
LIG_SH2_STAP1 | 431 | 435 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 394 | 397 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.484 |
LIG_SH3_2 | 417 | 422 | PF14604 | 0.643 |
LIG_SH3_3 | 342 | 348 | PF00018 | 0.644 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.601 |
LIG_SUMO_SIM_par_1 | 323 | 332 | PF11976 | 0.528 |
LIG_SUMO_SIM_par_1 | 39 | 45 | PF11976 | 0.463 |
LIG_TRAF2_1 | 205 | 208 | PF00917 | 0.440 |
LIG_TRAF2_1 | 372 | 375 | PF00917 | 0.529 |
LIG_TRFH_1 | 212 | 216 | PF08558 | 0.394 |
LIG_WRC_WIRS_1 | 209 | 214 | PF05994 | 0.361 |
LIG_WRC_WIRS_1 | 68 | 73 | PF05994 | 0.480 |
MOD_CDK_SPxxK_3 | 161 | 168 | PF00069 | 0.506 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.521 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.588 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.669 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.475 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.417 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.551 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.424 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.521 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.529 |
MOD_CK2_1 | 288 | 294 | PF00069 | 0.683 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.594 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.648 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.619 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.635 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.562 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.598 |
MOD_GlcNHglycan | 330 | 334 | PF01048 | 0.569 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.595 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.663 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.649 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.502 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.614 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.477 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.596 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.392 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.451 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.649 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.559 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.500 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.482 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.622 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.441 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.453 |
MOD_N-GLC_2 | 108 | 110 | PF02516 | 0.544 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.628 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.521 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.359 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.544 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.637 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.521 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.448 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.393 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.629 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.396 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.636 |
MOD_NEK2_2 | 300 | 305 | PF00069 | 0.508 |
MOD_NEK2_2 | 397 | 402 | PF00069 | 0.563 |
MOD_PIKK_1 | 130 | 136 | PF00454 | 0.654 |
MOD_PIKK_1 | 150 | 156 | PF00454 | 0.484 |
MOD_PIKK_1 | 36 | 42 | PF00454 | 0.472 |
MOD_PK_1 | 118 | 124 | PF00069 | 0.534 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.494 |
MOD_PKA_2 | 218 | 224 | PF00069 | 0.612 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.633 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.567 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.595 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.502 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.590 |
MOD_Plk_1 | 315 | 321 | PF00069 | 0.587 |
MOD_Plk_1 | 397 | 403 | PF00069 | 0.500 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.534 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.458 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.537 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.398 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.650 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.728 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.467 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.530 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.394 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.609 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.501 |
MOD_SUMO_rev_2 | 423 | 430 | PF00179 | 0.655 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.633 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.497 |
TRG_ER_diArg_1 | 10 | 12 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 222 | 224 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 401 | 404 | PF00400 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 222 | 227 | PF00026 | 0.536 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6G3 | Leptomonas seymouri | 36% | 100% |
A0A3Q8ICP2 | Leishmania donovani | 99% | 100% |
A4HD34 | Leishmania braziliensis | 73% | 100% |
E9AWI2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QAY8 | Leishmania major | 93% | 100% |
V5ARA2 | Trypanosoma cruzi | 23% | 100% |